@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_head {
  this: np:hasAssertion dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion;
    np:hasProvenance dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance;
    np:hasPublicationInfo dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion a np:Assertion .
  
  dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance a np:Provenance .
  
  dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN9f1a2f687a1ac8f664496660d0252c31 sio:SIO_000628 miriam-gene:672, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance {
  dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion dcterms:description
      "[To determine whether there are any molecular markers that might help explain this paradox between pathologically aggressive neoplasms in patients with HBC and the lack of extreme clinically aggressive disease, we studied several molecular parameters in a group of 34 breast cancer patients with mutations in either the BRCA1 or BRCA2 tumor suppressor genes and compared them with a group of 20 breast cancer patients with non-HBC.]. 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:9781655;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}