@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0> .
@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:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_head {
  this: np:hasAssertion dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion;
    np:hasProvenance dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance;
    np:hasPublicationInfo dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion a np:Assertion .
  
  dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance a np:Provenance .
  
  dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion {
  miriam-gene:2882 a ncit:C16612 .
  
  lld:C0677886 a ncit:C7057 .
  
  dgn-gda:DGN5d2c1b7dbcd2fa2043d4aa1a38b5a746 sio:SIO_000628 miriam-gene:2882, lld:C0677886;
    a sio:SIO_001121 .
}

dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance {
  dgn-np:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_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 &lt; 5 × 10(-8).]. 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:25581431;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:15+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" .
}