@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o> .
@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:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_head {
  this: np:hasAssertion dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_assertion;
    np:hasProvenance dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_provenance;
    np:hasPublicationInfo dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_assertion a np:Assertion .
  
  dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_provenance a np:Provenance .
  
  dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C1883486 a ncit:C7057 .
  
  dgn-gda:DGN409f44b195223a9af5b6ae6109f15208 sio:SIO_000628 miriam-gene:7515, lld:C1883486;
    a sio:SIO_001121 .
}

dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_provenance {
  dgn-np:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_assertion dcterms:description
      "[Although there were no significant (p > 0.05) differences in the frequencies of genotypes or alleles of hOGG1 genes between patients and controls, the frequency of the XRCC1 399Gln allele was significantly greater in endometrial cancer patients compared with controls (p = 0.033) with an odds ratio of 1.39 (95% confidence interval 0.99 to 1.95).]. 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:21866464;
    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:NP457828.RAn7uq6LnOT0HhZ80dLVo1EocetYO1p1ri_0OINaO7G4o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:33+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" .
}