@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M> .
@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:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_head {
  this: np:hasAssertion dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_assertion;
    np:hasProvenance dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_provenance;
    np:hasPublicationInfo dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_assertion a np:Assertion .
  
  dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_provenance a np:Provenance .
  
  dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNade259cc009231a76a26a24525aa0f45 sio:SIO_000628 miriam-gene:7515, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_provenance {
  dgn-np:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_assertion dcterms:description
      "[In addition, breast cancer risk was significantly associated with an increasing number of combined variant alleles of XRCC1 Arg194Trp, XRCC3 Thr241Met, and ERCC4/XPF Arg415Gln in a four-level model (P(trend) = 0.04): OR = 1.0 for those without a variant allele (referent group); OR = 1.04 (95% CI = 0.67-1.61) for those with one variant allele; OR = 1.38 (95% CI = 0.83-2.29) for those with two variant alleles; and age-adjusted OR = 2.60 (95% CI = 1.03-6.59) for those with three or more variant alleles after adjustment for age, family history, age at menarche, age at first live birth, and body mass index.]. 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:14652281;
    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:NP423014.RAf_kY92EoOcTDJRTeUy6dbfpiiV1hiQJFUFdj7Zs2p3M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:57+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" .
}