@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM> .
@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:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_head {
  this: np:hasAssertion dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion;
    np:hasProvenance dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_provenance;
    np:hasPublicationInfo dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion a np:Assertion .
  
  dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_provenance a np:Provenance .
  
  dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN8fa68d261b15d4ecdfe53672745252a6 sio:SIO_000628 miriam-gene:672, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_provenance {
  dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion dcterms:description
      "[At least one of ten patients with ovarian cancer is estimated to develop their tumor because of heredity with the breast and ovarian cancer syndrome due to mutations in the BRCA1 and BRCA2 genes and hereditary nonpolyposis colorectal cancer (HNPCC) being the major genetic causes.]. 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:17343610;
    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:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:16+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" .
}