@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk> .
@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:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_head {
  this: np:hasAssertion dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_assertion;
    np:hasProvenance dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_provenance;
    np:hasPublicationInfo dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_assertion a np:Assertion .
  
  dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_provenance a np:Provenance .
  
  dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNceee4f829bfca93c6e8cbba7ce88e8d5 sio:SIO_000628 miriam-gene:672, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_provenance {
  dgn-np:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_assertion dcterms:description
      "[Eligibility criterion for most of these trials was documented mutations in BRCA1 and 2 or future breast cancer risk predicted by family history or models, thereby possibly excluding women at significantly elevated risk that testing failed to identify or whose risk is not adequately reflected based on current models used in risk assessment.]. 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:15648188;
    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:NP476113.RAoZIbpUdZiTnqckEFqE6DeEumEKybRAk250UNBTEgwyk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:20+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" .
}