@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec
> .
@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:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_head
{
this:
np:hasAssertion
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_assertion
;
np:hasProvenance
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_provenance
;
np:hasPublicationInfo
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_assertion
a
np:Assertion
.
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_provenance
a
np:Provenance
.
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_assertion
{
miriam-gene:171024
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGNe1294d1f315f8d1e9c1f384e9f4e386b
sio:SIO_000628
miriam-gene:171024
,
lld:C0677886
;
a
sio:SIO_001122
.
}
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_provenance
{
dgn-np:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_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:NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_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" .
}