@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks
> .
@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:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_head
{
this:
np:hasAssertion
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_assertion
;
np:hasProvenance
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_provenance
;
np:hasPublicationInfo
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_assertion
a
np:Assertion
.
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_provenance
a
np:Provenance
.
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_assertion
{
miriam-gene:6770
a
ncit:C16612
.
lld:C0014170
a
ncit:C7057
.
dgn-gda:DGNe5364b621d16b6640d5c888ae3862482
sio:SIO_000628
miriam-gene:6770
,
lld:C0014170
;
a
sio:SIO_001122
.
}
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_provenance
{
dgn-np:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_assertion
dcterms:description
"[Genetic variants in CYP11A1 may influence endometrial cancer risk or may be markers for causal variants elsewhere. Polymorphisms in StAR are not associated with endometrial cancer risk, but further research is needed.]. 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:20199803
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP92094.RAUK5winXP7X6J0grvAZbHvanCSO87W8IwOjpwskfMhks130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}