@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M> .
@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:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_head {
  this: np:hasAssertion dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion;
    np:hasProvenance dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_provenance;
    np:hasPublicationInfo dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion a np:Assertion .
  
  dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_provenance a np:Provenance .
  
  dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0018553 a ncit:C7057 .
  
  dgn-gda:DGN262851a1cda08558f090651f3a5dbe9c sio:SIO_000628 miriam-gene:675, lld:C0018553;
    a sio:SIO_001121 .
}

dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_provenance {
  dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion dcterms:description
      "[Whilst breast cancer occurring in patients in Li-Fraumeni and Cowden's syndrome families is of great importance, the more frequent scenario is that of women, or indeed of men, presenting with breast cancer with an underlying germline mutation in BRCA1 or BRCA2.]. 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:19027287;
    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:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:12+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: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" .
}