@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg> .
@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:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_head {
  this: np:hasAssertion dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_assertion;
    np:hasProvenance dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_provenance;
    np:hasPublicationInfo dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_assertion a np:Assertion .
  
  dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_provenance a np:Provenance .
  
  dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNc39dbdf782d06d170609ec8746ba7f58 sio:SIO_000628 miriam-gene:672, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_provenance {
  dgn-np:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_assertion dcterms:description
      "[Women who have inherited a deleterious mutation in the BRCA1 or BRCA2 gene and those with the Lynch syndrome (hereditary nonpolyposis colorectal cancer) have the highest risk of developing ovarian cancer but account for only approximately 10% of those with the disease.]. 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:21521830;
    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:NP889862.RAjU22VXdlwdXyWkPfsGaaWXcSE4eIOiyfD_cIngXxhGg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:27+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" .
}