@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8
> .
@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:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_head
{
this:
np:hasAssertion
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_assertion
;
np:hasProvenance
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_assertion
a
np:Assertion
.
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_provenance
a
np:Provenance
.
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0153452
a
ncit:C7057
.
dgn-gda:DGN12436cfc1f70a3a6eb10df4e1a964028
sio:SIO_000628
miriam-gene:1543
,
lld:C0153452
;
a
sio:SIO_001121
.
}
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_provenance
{
dgn-np:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_assertion
dcterms:description
"[These results suggest that the Val allele of CYP1A1 Ile462Val polymorphism and the Pro allele of TP53 Arg72Pro polymorphism contribute to an increased risk of GBC among Japanese women and men, respectively.]. 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:17531965
;
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:NP297137.RAs5yt-V3Jhvrh932ccLklduJpYB_dThg036OL3PN2ZH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
}