@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8> .
@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:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_head {
  this: np:hasAssertion dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_assertion;
    np:hasProvenance dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_provenance;
    np:hasPublicationInfo dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_assertion a np:Assertion .
  
  dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_provenance a np:Provenance .
  
  dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN2ecb1b1625cef6c9c263eea0039716fb sio:SIO_000628 miriam-gene:7515, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_provenance {
  dgn-np:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_assertion dcterms:description
      "[Thus, the Gln allele was significantly more frequent in breast cancer cases (allele frequency, 0.52) than in controls (allele frequency, 0.35), suggesting that XRCC1 399Gln may enhance the risk of breast cancer.]. 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:18357393;
    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:NP661840.RA8637ST2ucongqMa0XNZRPAnE4yXbc4BjSI7-HfAdAc8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:45+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" .
}