@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_head
{
this:
np:hasAssertion
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion
;
np:hasProvenance
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion
a
np:Assertion
.
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance
a
np:Provenance
.
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion
{
miriam-gene:54361
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN9aa9e7d3efdf847368572ec3eab6dd27
sio:SIO_000628
miriam-gene:54361
,
lld:C0677886
;
a
sio:SIO_001122
.
}
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance
{
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion
dcterms:description
"[Variants at 1p36 (nearest gene, WNT4), 4q26 (SYNPO2), 9q34.2 (ABO) and 17q11.2 (ATAD5) were associated with EOC risk, and at 1p34.3 (RSPO1) and 6p22.1 (GPX6) variants were specifically associated with the serous EOC subtype, all with P < 5 × 10(-8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:25581431
;
prov:wasDerivedFrom
dgn-void:gwascat-2016
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:gwascat-2016
pav:importedOn
"2016-01-27"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:13+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}