@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw> .
@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:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_head {
  this: np:hasAssertion dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_assertion;
    np:hasProvenance dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_provenance;
    np:hasPublicationInfo dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_assertion a np:Assertion .
  
  dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_provenance a np:Provenance .
  
  dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0003469 a ncit:C7057 .
  
  dgn-gda:DGN9446f0de36454e79e9432163ec04fe02 sio:SIO_000628 miriam-gene:675, lld:C0003469;
    a sio:SIO_001121 .
}

dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_provenance {
  dgn-np:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_assertion dcterms:description
      "[As such, their identification is essential to reduce the risk of disease in healthy carriers, as well as in carriers who have already developed the disease because they are at increased risk for a second malignancy; moreover, noncarriers of BRCA1 and BRCA2 mutated families can be spared anxiety and unnecessary medical interventions.]. 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:11920643;
    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:NP720538.RAGe_8yYkdgzCbqsV1CD0O2t4V6exuLy3RDbdo1dVMVdw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:17+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" .
}