@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA> .
@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:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_head {
  this: np:hasAssertion dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion;
    np:hasProvenance dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_provenance;
    np:hasPublicationInfo dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion a np:Assertion .
  
  dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_provenance a np:Provenance .
  
  dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion {
  miriam-gene:55655 a ncit:C16612 .
  
  lld:C0281267 a ncit:C7057 .
  
  dgn-gda:DGN3a1b4e23fa9b1dbd0bf6d9afdeaa9eba sio:SIO_000628 miriam-gene:55655, lld:C0281267;
    a sio:SIO_001121 .
}

dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_provenance {
  dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion dcterms:description
      "[Recent studies have demonstrated that heterozygous carriers of the NBS1 657del5 mutation have an increased risk for familial and bilateral breast cancer, but similar studies in consecutive breast cancer patients were inconclusive.]. 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:16770759;
    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:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:05+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" .
}