Knowledge Media Panel U Toronto, Sept 30 2010
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Transcript of Knowledge Media Panel U Toronto, Sept 30 2010
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What is inside our full-text articles, and how do we improve access to it?Or: Stories, that persuade with data.
Anita de Waard, [email protected] Disruptive Technologies Director, Elsevier Labs
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Model of a paper: “Scientific articles are stories...
2
The Story of Goldilocks and the Three Bears
Story Grammar Paper The AXH Domain of Ataxin-1 Mediates Neurodegeneration through Its Interaction with Gfi-1/Senseless Proteins
Once upon a time Time Setting Background The mechanisms mediating SCA1 pathogenesis are still not fully understood, but some general principles have emerged.
a little girl named Goldilocks Characters
Setting
Objects of study the Drosophila Atx-1 homolog (dAtx-1) which lacks a polyQ tract,
She went for a walk in the forest. Pretty soon, she came upon a house.
Location
Setting
Experimental setup
studied and compared in vivo effects and interactions to those of the human protein
She knocked and, when no one answered,
Goal Theme Researchgoal
Gain insight into how Atx-1's function contributes to SCA1 pathogenesis. How these interactions might contribute to the disease process and how they might cause toxicity in only a subset of neurons in SCA1 is not fully understood.she walked right in. Attempt
Theme
Hypothesis Atx-1 may play a role in the regulation of gene expression
At the table in the kitchen, there were three bowls of porridge.
Name Episode 1 Name dAtX-1 and hAtx-1 Induce Similar Phenotypes When Overexpressed in Files
Goldilocks was hungry. Subgoal
Episode 1
Subgoal test the function of the AXH domainShe tasted the porridge from the first bowl.
Attempt
Episode 1
Method overexpressed dAtx-1 in flies using the GAL4/UAS system (Brand and Perrimon, 1993) and compared its effects to those of hAtx-1.
This porridge is too hot! she exclaimed.
Outcome
Episode 1
Results Overexpression of dAtx-1 by Rhodopsin1(Rh1)-GAL4, which drives expression in the differentiated R1-R6 photoreceptor cells (Mollereau et al., 2000 and O'Tousa et al., 1985), results in neurodegeneration in the eye, as does overexpression of hAtx-1[82Q]. Although at 2 days after eclosion, overexpression of either Atx-1 does not show obvious morphological changes in the photoreceptor cells
So, she tasted the porridge from the second bowl.
Activity
Episode 1
Data (data not shown),
This porridge is too cold, she said
Outcome
Episode 1
Results both genotypes show many large holes and loss of cell integrity at 28 days
So, she tasted the last bowl of porridge.
Activity
Episode 1
Data (Figures 1B-1D).
Ahhh, this porridge is just right, she said happily and
Outcome
Episode 1
Results Overexpression of dAtx-1 using the GMR-GAL4 driver also induces eye abnormalities. The external structures of the eyes that overexpress dAtx-1 show disorganized ommatidia and loss of interommatidial bristles she ate it all up.
Episode 1
Data (Figure 1F),
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Model of a paper: “Scientific articles are stories...
2
The Story of Goldilocks and the Three Bears
Story Grammar Paper The AXH Domain of Ataxin-1 Mediates Neurodegeneration through Its Interaction with Gfi-1/Senseless Proteins
Once upon a time Time Setting Background The mechanisms mediating SCA1 pathogenesis are still not fully understood, but some general principles have emerged.
a little girl named Goldilocks Characters
Setting
Objects of study the Drosophila Atx-1 homolog (dAtx-1) which lacks a polyQ tract,
She went for a walk in the forest. Pretty soon, she came upon a house.
Location
Setting
Experimental setup
studied and compared in vivo effects and interactions to those of the human protein
She knocked and, when no one answered,
Goal Theme Researchgoal
Gain insight into how Atx-1's function contributes to SCA1 pathogenesis. How these interactions might contribute to the disease process and how they might cause toxicity in only a subset of neurons in SCA1 is not fully understood.she walked right in. Attempt
Theme
Hypothesis Atx-1 may play a role in the regulation of gene expression
At the table in the kitchen, there were three bowls of porridge.
Name Episode 1 Name dAtX-1 and hAtx-1 Induce Similar Phenotypes When Overexpressed in Files
Goldilocks was hungry. Subgoal
Episode 1
Subgoal test the function of the AXH domainShe tasted the porridge from the first bowl.
Attempt
Episode 1
Method overexpressed dAtx-1 in flies using the GAL4/UAS system (Brand and Perrimon, 1993) and compared its effects to those of hAtx-1.
This porridge is too hot! she exclaimed.
Outcome
Episode 1
Results Overexpression of dAtx-1 by Rhodopsin1(Rh1)-GAL4, which drives expression in the differentiated R1-R6 photoreceptor cells (Mollereau et al., 2000 and O'Tousa et al., 1985), results in neurodegeneration in the eye, as does overexpression of hAtx-1[82Q]. Although at 2 days after eclosion, overexpression of either Atx-1 does not show obvious morphological changes in the photoreceptor cells
So, she tasted the porridge from the second bowl.
Activity
Episode 1
Data (data not shown),
This porridge is too cold, she said
Outcome
Episode 1
Results both genotypes show many large holes and loss of cell integrity at 28 days
So, she tasted the last bowl of porridge.
Activity
Episode 1
Data (Figures 1B-1D).
Ahhh, this porridge is just right, she said happily and
Outcome
Episode 1
Results Overexpression of dAtx-1 using the GMR-GAL4 driver also induces eye abnormalities. The external structures of the eyes that overexpress dAtx-1 show disorganized ommatidia and loss of interommatidial bristles she ate it all up.
Episode 1
Data (Figure 1F),
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“...that persuade (editors/authors/readers!)...”
3
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“...that persuade (editors/authors/readers!)...”
3
Aristotle QuintilianQuintilian Scientific Paper
prooimion Introduction/ exordium
The introduction of a speech, where one announces the subject and purpose of the discourse, and where one usually employs the persuasive appeal to ethos in order to establish credibility with the audience.
Introduction: positioning
prothesisStatement of Facts/narratio
The speaker here provides a narrative account of what has happened and generally explains the nature of the case.
Introduction: research question
Summary/ propostitio
The propositio provides a brief summary of what one is about to speak on, or concisely puts forth the charges or accusation. Summary of contents
pistis Proof/ confirmatio
The main body of the speech where one offers logical arguments as proof. The appeal to logos is emphasized here.
Results
Refutation/ refutatio
As the name connotes, this section of a speech was devoted to answering the counterarguments of one's opponent. Related Work
epilogos peroratio Following the refutatio and concluding the classical oration, the peroratio conventionally employed appeals through pathos, and often included a summing up.
Discussion: summary, implications.
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“...that persuade (editors/authors/readers!)...”
3
Aristotle QuintilianQuintilian Scientific Paper
prooimion Introduction/ exordium
The introduction of a speech, where one announces the subject and purpose of the discourse, and where one usually employs the persuasive appeal to ethos in order to establish credibility with the audience.
Introduction: positioning
prothesisStatement of Facts/narratio
The speaker here provides a narrative account of what has happened and generally explains the nature of the case.
Introduction: research question
Summary/ propostitio
The propositio provides a brief summary of what one is about to speak on, or concisely puts forth the charges or accusation. Summary of contents
pistis Proof/ confirmatio
The main body of the speech where one offers logical arguments as proof. The appeal to logos is emphasized here.
Results
Refutation/ refutatio
As the name connotes, this section of a speech was devoted to answering the counterarguments of one's opponent. Related Work
epilogos peroratio Following the refutatio and concluding the classical oration, the peroratio conventionally employed appeals through pathos, and often included a summing up.
Discussion: summary, implications.
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“... with data.”
4
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“... with data.”
4
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“... with data.”
4
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So how do we improve access to these?
5
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So how do we improve access to these?
5
1.1. Better access to ‘story’ elements:
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So how do we improve access to these?
5
1.1. Better access to ‘story’ elements: • Learn from Fairy Tale annotation/Proppian Markup?
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So how do we improve access to these?
5
1.1. Better access to ‘story’ elements: • Learn from Fairy Tale annotation/Proppian Markup?
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So how do we improve access to these?
5
1.1. Better access to ‘story’ elements: • Learn from Fairy Tale annotation/Proppian Markup?
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So how do we improve access to these?
5
1.1. Better access to ‘story’ elements: • Learn from Fairy Tale annotation/Proppian Markup?• W3C HCLS SiG Scientific discourse structure:
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So how do we improve access to these?
5
1.1. Better access to ‘story’ elements: • Learn from Fairy Tale annotation/Proppian Markup?• W3C HCLS SiG Scientific discourse structure:
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1.2. Element access through Linked Data:
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1.2. Element access through Linked Data:
<ce:section id=#123>
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1.2. Element access through Linked Data:
<ce:section id=#123> mice like cheesethis says
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1.2. Element access through Linked Data:
<ce:section id=#123>
said @anita on September 8, 2010
mice like cheesethis says
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but we all know she was wrong then
1.2. Element access through Linked Data:
<ce:section id=#123>
said @anita on September 8, 2010
mice like cheesethis says
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but we all know she was wrong then
1.2. Element access through Linked Data:
<ce:section id=#123>
said @anita on September 8, 2010
the xml is fixed, but the structure is open!
mice like cheesethis says
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allows for layers of annotation
but we all know she was wrong then
1.2. Element access through Linked Data:
<ce:section id=#123>
said @anita on September 8, 2010
the xml is fixed, but the structure is open!
mice like cheesethis says
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
Result
![Page 30: Knowledge Media Panel U Toronto, Sept 30 2010](https://reader034.fdocuments.net/reader034/viewer/2022051514/549596d1b479591b158b461a/html5/thumbnails/30.jpg)
2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
Result
Implication
![Page 31: Knowledge Media Panel U Toronto, Sept 30 2010](https://reader034.fdocuments.net/reader034/viewer/2022051514/549596d1b479591b158b461a/html5/thumbnails/31.jpg)
2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
Result
Implication
Goal
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
Result
Implication
Goal
Reg-Implication
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
Result
Implication
Goal
Reg-Implication
Conceptual knowledge
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2.1. Improve access to persuasive elements:Identify key rhetorical elements in scientific text:
7
Both seminomas and the EC component of nonseminomas share features with ES cells. To exclude that the detection of miR-371-3 merely reflects its expression pattern in ES cells, we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004). In many of the m i R - 3 7 1 - 3 e x p r e s s i n g s e m i n o m a s a n d nonseminomas, miR-302a-d was undetectable (Figs S7 and S8), suggesting that miR-371-3 expression is a selective event during tumorigenesis.
Both seminomas and the EC component of nonseminomas share features with ES cells.To exclude thatthe detection of miR-371-3 merely reflects its expression pattern in ES cells,we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),suggesting thatmiR-371-3 expression is a selective event during tumorigenesis.
Fact
Hypothesis
Method
Result
Implication
Goal
Reg-Implication
Conceptual knowledge
ExperimentalEvidence
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2.2. Realms in experimental discourse
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(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
2.2. Realms in experimental discourse
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(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) a. To exclude that
2.2. Realms in experimental discourse
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(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) c. we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).
(3) a. In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),
(2) a. To exclude that
2.2. Realms in experimental discourse
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(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) c. we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).
(3) a. In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),
(2) a. To exclude that (3) b. suggesting that
2.2. Realms in experimental discourse
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(3) c. miR-371-3 expression is a selective event during tumorigenesis.
(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) c. we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).
(3) a. In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),
(2) a. To exclude that (3) b. suggesting that
2.2. Realms in experimental discourse
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(3) c. miR-371-3 expression is a selective event during tumorigenesis.
(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) c. we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).
(3) a. In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),
Concepts, models, ‘facts’
(2) a. To exclude that (3) b. suggesting that
2.2. Realms in experimental discourse
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(3) c. miR-371-3 expression is a selective event during tumorigenesis.
(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) c. we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).
(3) a. In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),
Concepts, models, ‘facts’
Experiment
(2) a. To exclude that (3) b. suggesting that
2.2. Realms in experimental discourse
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(3) c. miR-371-3 expression is a selective event during tumorigenesis.
(1) Both seminomas and the EC component of nonseminomas share features with ES cells.
(2) b. the detection of miR-371-3 merely reflects its expression pattern in ES cells,
(2) c. we tested by RPA miR-302a-d, another ES cells-specific miRNA cluster (Suh et al, 2004).
(3) a. In many of the miR-371-3 expressing seminomas and nonseminomas, miR-302a-d was undetectable (Figs S7 and S8),
Concepts, models, ‘facts’
Experiment
Transitions(2) a. To exclude that (3) b. suggesting that
2.2. Realms in experimental discourse
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2.3. Hypotheses, Evidence and Relationships:
9
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2.3. Hypotheses, Evidence and Relationships:
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2.3. Hypotheses, Evidence and Relationships:
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2.3. Hypotheses, Evidence and Relationships:
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2.3. Hypotheses, Evidence and Relationships:
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2.3. Hypotheses, Evidence and Relationships:
Hypothesis 22: Intramembrenous Aβ dimer may be toxic.
Derived from: POSTAT_CONTRIBUTION(This essay explores the possibility that a fraction of these Abeta peptides never leave the membrane lipid bilayer after they are generated, but instead exert their toxic effects by competing with and compromising the functions of intramembranous segments of membrane-bound proteins that serve many critical functions.
9
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2.3. Hypotheses, Evidence and Relationships:
9
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2.3. Hypotheses, Evidence and Relationships:
9
• Collective of groups working on representing scientific text as – discourse elements– linked by rhetorical relationships– connected to data
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2.3. Hypotheses, Evidence and Relationships:
9
• Collective of groups working on representing scientific text as – discourse elements– linked by rhetorical relationships– connected to data
• Current efforts: – W3C HCLS SiG: development of a Rhetorical Document Structure– Unification of ScholOnto, CiTO, SWAN, SALT relations
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2.3. Hypotheses, Evidence and Relationships:
9
• Collective of groups working on representing scientific text as – discourse elements– linked by rhetorical relationships– connected to data
• Current efforts: – W3C HCLS SiG: development of a Rhetorical Document Structure– Unification of ScholOnto, CiTO, SWAN, SALT relations
• Developing an Annotation Framework with Harvard/MGH:– Access to collection of full-text content on Alzheimer’s– Allow standoff annotation through Harvard’s Annotation Ontology– Run several hypothesis/event identification tools - access through
U-Compare, UMIA, SciKnowMine– Allow layering of annotations– Test with users in Alzheimer community!
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2.4. Three dimensions of annotation:
measure
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2.4. Three dimensions of annotation:
measure
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document
claim
triple
entity
collection
Granularity2.4. Three dimensions of annotation:
measure
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document
claim
triple
entity
collection
Granularity2.4. Three dimensions of annotation:
automated
manual
semi-automated
Meansmeasure
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document
claim
triple
entity
collection
Granularity2.4. Three dimensions of annotation:
reader/curator/data miningtypesetter/productionauthor/editor
Moment
automated
manual
semi-automated
Meansmeasure
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document
claim
triple
entity
collection
Granularity2.4. Three dimensions of annotation:
Entity Markupreader/curator/data miningtypesetter/productionauthor/editor
Moment
automated
manual
semi-automated
Meansmeasure
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document
claim
triple
entity
collection
Granularity2.4. Three dimensions of annotation:
Hypothesis markup
Entity Markupreader/curator/data miningtypesetter/productionauthor/editor
Moment
automated
manual
semi-automated
Meansmeasure
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document
claim
triple
entity
collection
Granularity2.4. Three dimensions of annotation:
Hypothesis markup
Entity Markupreader/curator/data miningtypesetter/productionauthor/editor
Moment
automated
manual
semi-automated
Meansmeasure
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3.1. Research data
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... gets created...
3.1. Research data
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... gets created... ... and destroyed!
3.1. Research data
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3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
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3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
1. Research: Each item in the system has metadata (including provenance) and relations to other data items added to it.
metadata
metadata
metadata
metadata
metadata
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3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
1. Research: Each item in the system has metadata (including provenance) and relations to other data items added to it.
metadata
metadata
metadata
metadata
metadata
2. Workflow: All data items created in the lab are added to a (lab-owned) workflow system.
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3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
1. Research: Each item in the system has metadata (including provenance) and relations to other data items added to it.
metadata
metadata
metadata
metadata
metadata
2. Workflow: All data items created in the lab are added to a (lab-owned) workflow system.
Rats were subjected to two grueling tests(click on fig 2 to see underlying data). These results suggest that the neurological pain pro-
3. Authoring: A paper is written in an authoring tool which can pull data with provenance from the workflow tool in the appropriate representation into the document.
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3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
1. Research: Each item in the system has metadata (including provenance) and relations to other data items added to it.
metadata
metadata
metadata
metadata
metadata
2. Workflow: All data items created in the lab are added to a (lab-owned) workflow system.
4. Editing and review: Once the co-authors agree, the paper is ‘exposed’ to the editors, who in turn expose it to reviewers. Reports are stored in the authoring/editing system, the paper gets updated, until it is validated.
Review
EditRevise
Rats were subjected to two grueling tests(click on fig 2 to see underlying data). These results suggest that the neurological pain pro-
3. Authoring: A paper is written in an authoring tool which can pull data with provenance from the workflow tool in the appropriate representation into the document.
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3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
1. Research: Each item in the system has metadata (including provenance) and relations to other data items added to it.
metadata
metadata
metadata
metadata
metadata
5. Publishing and distribution: When a paper is published, a collection of validated information is exposed to the world. It remains connected to its related data item, and its heritage can be traced.
2. Workflow: All data items created in the lab are added to a (lab-owned) workflow system.
4. Editing and review: Once the co-authors agree, the paper is ‘exposed’ to the editors, who in turn expose it to reviewers. Reports are stored in the authoring/editing system, the paper gets updated, until it is validated.
Review
EditRevise
Rats were subjected to two grueling tests(click on fig 2 to see underlying data). These results suggest that the neurological pain pro-
3. Authoring: A paper is written in an authoring tool which can pull data with provenance from the workflow tool in the appropriate representation into the document.
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Some other publisher
6. User applications: distributed applications run on this ‘exposed data’ universe.
3.2. Data-driven papers? Work done with Ed Hovy, Phil Bourne, Gully Burns and Cartic Ramakrishnan
1. Research: Each item in the system has metadata (including provenance) and relations to other data items added to it.
metadata
metadata
metadata
metadata
metadata
5. Publishing and distribution: When a paper is published, a collection of validated information is exposed to the world. It remains connected to its related data item, and its heritage can be traced.
2. Workflow: All data items created in the lab are added to a (lab-owned) workflow system.
4. Editing and review: Once the co-authors agree, the paper is ‘exposed’ to the editors, who in turn expose it to reviewers. Reports are stored in the authoring/editing system, the paper gets updated, until it is validated.
Review
EditRevise
Rats were subjected to two grueling tests(click on fig 2 to see underlying data). These results suggest that the neurological pain pro-
3. Authoring: A paper is written in an authoring tool which can pull data with provenance from the workflow tool in the appropriate representation into the document.
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3.3. Small step: ScienceDirect app store
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3.4. Social Change! Some next steps:
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3.4. Social Change! Some next steps:
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• January 2011: ‘Beyond the PDF’ workshop, Phil Bourne: linking data to papers; develop virtual community around that
3.4. Social Change! Some next steps:
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• January 2011: ‘Beyond the PDF’ workshop, Phil Bourne: linking data to papers; develop virtual community around that
• June 2011: ‘Executable Paper Challenge’ @ ICCS: ask computer scientists to submit ideas for ‘executable papers’ - embedded code or data
3.4. Social Change! Some next steps:
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• January 2011: ‘Beyond the PDF’ workshop, Phil Bourne: linking data to papers; develop virtual community around that
• June 2011: ‘Executable Paper Challenge’ @ ICCS: ask computer scientists to submit ideas for ‘executable papers’ - embedded code or data
• August 2011: Dagstuhl Workshop ‘Future of Research Communications’ (Ed Hovy, Ivan Herman, Tim Clark, Anita de Waard):
3.4. Social Change! Some next steps:
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• January 2011: ‘Beyond the PDF’ workshop, Phil Bourne: linking data to papers; develop virtual community around that
• June 2011: ‘Executable Paper Challenge’ @ ICCS: ask computer scientists to submit ideas for ‘executable papers’ - embedded code or data
• August 2011: Dagstuhl Workshop ‘Future of Research Communications’ (Ed Hovy, Ivan Herman, Tim Clark, Anita de Waard):
–Involve key parties (scientists, publishers, funding bodies, libraries) to map out main bottlenecks
3.4. Social Change! Some next steps:
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• January 2011: ‘Beyond the PDF’ workshop, Phil Bourne: linking data to papers; develop virtual community around that
• June 2011: ‘Executable Paper Challenge’ @ ICCS: ask computer scientists to submit ideas for ‘executable papers’ - embedded code or data
• August 2011: Dagstuhl Workshop ‘Future of Research Communications’ (Ed Hovy, Ivan Herman, Tim Clark, Anita de Waard):
–Involve key parties (scientists, publishers, funding bodies, libraries) to map out main bottlenecks
–Write white paper
3.4. Social Change! Some next steps:
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• January 2011: ‘Beyond the PDF’ workshop, Phil Bourne: linking data to papers; develop virtual community around that
• June 2011: ‘Executable Paper Challenge’ @ ICCS: ask computer scientists to submit ideas for ‘executable papers’ - embedded code or data
• August 2011: Dagstuhl Workshop ‘Future of Research Communications’ (Ed Hovy, Ivan Herman, Tim Clark, Anita de Waard):
–Involve key parties (scientists, publishers, funding bodies, libraries) to map out main bottlenecks
–Write white paper–Implement?!
3.4. Social Change! Some next steps:
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Questions? Interested in collaboration?
http://elsatglabs.com/labs/anita
15