@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g> .
@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:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_head {
  this: np:hasAssertion dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_assertion ;
    np:hasProvenance dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_provenance ;
    np:hasPublicationInfo dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_assertion a np:Assertion .
  dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_provenance a np:Provenance .
  dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_assertion {
  miriam-gene:7517 a ncit:C16612 .
  lld:C0008626 a ncit:C7057 .
  dgn-gda:DGN910ac0d00971d2bbb3052cc6cfefbfbe sio:SIO_000628 miriam-gene:7517 , lld:C0008626 ;
    a sio:SIO_001121 .
}
dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_provenance {
  dgn-np:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_assertion dcterms:description "[We have studied the effect of genetic polymorphisms in the DNA repair genes hOGG1, XRCC1, XRCC3, ERCC2 and the MTHFR gene in the folate metabolism on the frequencies of cells with chromosomal aberrations (CA), chromosome-type aberrations (CSA), chromatid-type aberrations (CTA), chromatid breaks (CTB) and chromatid gaps (CTG) scored in peripheral blood lymphocytes from 651 Norwegian subjects of Caucasian descendant.]. 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:16997330 ;
    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:NP236561.RABCGKenlodfSGoqHhiOD3EqNeStGUdGe09u5ZWJUI19g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}