@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA> .
@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:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_head {
  this: np:hasAssertion dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion;
    np:hasProvenance dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_provenance;
    np:hasPublicationInfo dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion a np:Assertion .
  
  dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_provenance a np:Provenance .
  
  dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN0e7a037adab982b457e8726980a2dbeb sio:SIO_000628 miriam-gene:1312, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_provenance {
  dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion dcterms:description
      "[Although the study found that parental carrier status of certain CYP1B1 or COMT genotypes might be associated with daughter's breast cancer risk, the biological basis as well as independent confirmation of this finding need to be investigated in future larger family-based studies before making meaningful inferences.]. 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:15111770;
    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:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}