@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_assertion
a
np:Assertion
.
dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_provenance
a
np:Provenance
.
dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2264
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN5893432c57c212976aa0a26f6a8ec390
sio:SIO_000628
miriam-gene:2264
,
lld:C0242379
;
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.
}
dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_provenance
{
dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_assertion
dcterms:description
"[While we employed a comprehensive set of statistical tests, including those sensitive to the detection of differences in early survival, our data provide little evidence to support the tenet that the FGFR4 Gly388Arg polymorphism is a clinically useful marker for lung cancer prognosis.]. 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:17519899
;
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 .
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dgn-np:NP200421.RAA99oTiKNWxM8eGXbDC2PBQdW-xyankb_kd7P1S1z6cE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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http://orcid.org/0000-0002-9383-528X
> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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"v2.1.0" .
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