@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU> .
@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/v4.0.0/void/> .

dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_head {
  this: np:hasAssertion dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_assertion;
    np:hasProvenance dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_provenance;
    np:hasPublicationInfo dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_assertion a np:Assertion .
  
  dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_provenance a np:Provenance .
  
  dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNc7f4bd34433137919ebca10376cf10d6 sio:SIO_000628 miriam-gene:675, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_provenance {
  dgn-np:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_assertion dcterms:description
      "[Although the discovery of mutations on BRCA1 and BRCA2 genes associated with high breast cancer risk has given rise to screening and surveillance initiatives, there is little documentation on why high-risk women choose to enter screening programs.]. 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:19219540;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP720683.RAANMU1Rbv3QM0Od_u8qc0pr26hr54GNmdx2ZFShkDMuU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:12+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}