@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU> .
@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:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_head {
  this: np:hasAssertion dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion ;
    np:hasProvenance dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_provenance ;
    np:hasPublicationInfo dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion a np:Assertion .
  dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_provenance a np:Provenance .
  dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion {
  miriam-gene:672 a ncit:C16612 .
  lld:C0085183 a ncit:C7057 .
  dgn-gda:DGNc46d2c0f1f32d71fb3a10f38ccd4fe62 sio:SIO_000628 miriam-gene:672 , lld:C0085183 ;
    a sio:SIO_001121 .
}
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_provenance {
  dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_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:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:44+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" .
}