@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U> .
@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:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_head {
  this: np:hasAssertion dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_assertion ;
    np:hasProvenance dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_provenance ;
    np:hasPublicationInfo dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_assertion a np:Assertion .
  dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_provenance a np:Provenance .
  dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  lld:C0022593 a ncit:C7057 .
  dgn-gda:DGNa2a528fab1912b1cab49eb55af4573e6 sio:SIO_000628 miriam-gene:7515 , lld:C0022593 ;
    a sio:SIO_001121 .
}
dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_provenance {
  dgn-np:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_assertion dcterms:description "[Data from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.]. 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:17374727 ;
    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:NP691640.RA7yaIe6XfBp7l630hVPO2daEK8FC9pEAMyg1SQgVc93U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}