@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8> .
@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:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_head {
  this: np:hasAssertion dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_assertion;
    np:hasProvenance dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_provenance;
    np:hasPublicationInfo dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_assertion a np:Assertion .
  
  dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_provenance a np:Provenance .
  
  dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_assertion {
  miriam-gene:5889 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN7de0df9a4d00854cd473279f40a404f3 sio:SIO_000628 miriam-gene:5889, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_provenance {
  dgn-np:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_assertion dcterms:description
      "[RAD51C c.-13_14del27 was observed in one familial breast cancer case and c.774delT in one unselected ovarian cancer case, thus confirming that RAD51C mutations are implicated in breast and ovarian cancer predisposition, although their overall frequency seems to be low.]. 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:21750962;
    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:NP517649.RAY94KYYitLtrPhuAE2B166x9BDXnh8UAxWLSUKfn-4s8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:08+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" .
}