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http://rdf.disgenet.org/nanopublications.trig#NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_head
{
this:
np:hasAssertion
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_assertion
;
np:hasProvenance
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_provenance
;
np:hasPublicationInfo
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_provenance
a
np:Provenance
.
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_assertion
{
miriam-gene:4357
a
ncit:C16612
.
lld:C1834582
a
ncit:C7057
.
dgn-gda:DGN45ca59b3aa155c0dfc86ac5ae16e97a4
sio:SIO_000628
miriam-gene:4357
,
lld:C1834582
;
a
sio:SIO_001121
.
}
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_provenance
{
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_assertion
dcterms:description
"[In the genome-wide association study, three SNPs were associated significantly with shortened OS after multiple comparison adjustment: rs1656402 in the EIF4E2 gene (MST was 18.0 and 7.7 months for AG [n = 50] + AA [n = 40] and GG [n = 15], respectively; p = 8.4 × 10), rs1209950 in the ETS2 gene (MST = 17.7 and 7.4 months for CC [n = 94] and CT [n = 11] + TT [n = 0]; p = 2.8 × 10), and rs9981861 in the DSCAM gene (MST = 17.1 and 3.8 months for AA [n = 75] + AG [n = 26] and GG [n = 4]; p = 3.5 × 10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21079520
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP831754.RAinVPY-faGGTQA-xOowN6q42aXjNamb-quudBbiWgRVY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+02:00"^^
xsd:dateTime
;
dcterms:rights
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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pav:version
"v2.1.0" .
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