@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA> .
@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:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_head {
  this: np:hasAssertion dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_assertion;
    np:hasProvenance dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_provenance;
    np:hasPublicationInfo dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_assertion a np:Assertion .
  
  dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_provenance a np:Provenance .
  
  dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_assertion {
  miriam-gene:2068 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN4f115f87b4babc209fd03955e051a108 sio:SIO_000628 miriam-gene:2068, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_provenance {
  dgn-np:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_assertion dcterms:description
      "[Twenty-seven SNPs in VHL, HGF, IL18, PRKACB, ABCB1, CYP2C8, ERCC2, and ERCC1 previously associated with ovarian cancer outcome were genotyped in 10,084 invasive cases from 28 studies from the Ovarian Cancer Association Consortium with over 37,000-observed person-years and 4,478 deaths.]. 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:23513043;
    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:NP1061983.RAv06oLb0tFIUapT-wQMg6IO6Am5pq2bZWKAFg5dNFKRA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:47+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" .
}