@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc> .
@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#> .
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  this: np:hasAssertion dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_assertion ;
    np:hasProvenance dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_provenance ;
    np:hasPublicationInfo dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_assertion {
  miriam-gene:7517 a ncit:C16612 .
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dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_provenance {
  dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_assertion dcterms:description "[We used a case-control study design (162 cases and 302 controls) to test the association between three amino acid substitution variants of DNA repair genes (XRCC1 Arg194Trp, XRCC1 Arg399Gln, and XRCC3 Thr241Met) and breast cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP59494.RAJQteV1VWT42ZiecgxZnIxEx7MPOeQenl0ZJIPjklrwc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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