@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM> .
@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:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_head {
  this: np:hasAssertion dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion;
    np:hasProvenance dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance;
    np:hasPublicationInfo dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion a np:Assertion .
  
  dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance a np:Provenance .
  
  dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNfa0e86792b30ceec7b713ffd68231f31 sio:SIO_000628 miriam-gene:1029, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance {
  dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion dcterms:description
      "[Our findings show that few patients with BC and CMM who lacked family histories of these cancers are carriers of deleterious germline mutations in four of the five genes we examined.]. 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:17624602;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}