@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ> .
@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/v3.0.0/void/> .

dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_head {
  this: np:hasAssertion dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_assertion;
    np:hasProvenance dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_provenance;
    np:hasPublicationInfo dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_assertion a np:Assertion .
  
  dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_provenance a np:Provenance .
  
  dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0948303 a ncit:C7057 .
  
  dgn-gda:DGNe6c5a3a75cd0a3dfd2070f8a344a1c58 sio:SIO_000628 miriam-gene:672, lld:C0948303;
    a sio:SIO_001121 .
}

dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_provenance {
  dgn-np:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_assertion dcterms:description
      "[Hereditary breast-ovarian cancer (HBOC) syndrome and the associated BRCA1 and BRCA2 mutations are particularly prevalent in women of Jewish lineage, and specific BRCA1 and BRCA2 germline mutations have been linked with peritoneal carcinoma and HBOC syndrome in Jewish populations, especially those of Ashkenazi descent.]. 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:15516851;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP271354.RASIsUfWMOUE2TZzMFCb80rRSPrrhCmlizIelJiL4JqjQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:14+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}