@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U> .
@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:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_head {
  this: np:hasAssertion dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_assertion ;
    np:hasProvenance dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_provenance ;
    np:hasPublicationInfo dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_assertion a np:Assertion .
  dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_provenance a np:Provenance .
  dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_assertion {
  miriam-gene:675 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGN7ea57cc4c97522d73eedb1e3b1bfeee3 sio:SIO_000628 miriam-gene:675 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_provenance {
  dgn-np:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_assertion dcterms:description "[To detect potential novel gene defects that may contribute to hereditary BC susceptibility, 143 patients belonging to 143 Chilean families tested for BRCA1 and BRCA2 mutations were screened for mutations in RAD51, using conformational sensitive gel electrophoresis (CSGE) and DNA sequencing.]. 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:17889711 ;
    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:NP631370.RAkkekGcyDLqxGaGxrSxlURCHyWHqAKgMRvNCnv0T3i9U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:31+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" .
}