@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI> .
@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:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_head {
  this: np:hasAssertion dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_assertion ;
    np:hasProvenance dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_provenance ;
    np:hasPublicationInfo dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_assertion a np:Assertion .
  dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_provenance a np:Provenance .
  dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_assertion {
  miriam-gene:266790 a ncit:C16612 .
  lld:C0007102 a ncit:C7057 .
  dgn-gda:DGN9fdea68041a0a6a5d57ba358556034ef sio:SIO_000628 miriam-gene:266790 , lld:C0007102 ;
    a sio:SIO_001121 .
}
dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_provenance {
  dgn-np:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_assertion dcterms:description "[In a population-based case-control study of 537 cases and 866 controls, we investigated whether colon cancer was associated with genetic variations in UGT1A1 and UGT1A9 genes and we determined if those variations modify the association between colon cancer and dietary HCA and PAH exposure.]. 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:18675828 ;
    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:NP182544.RACVnJlCL4pdqWUnMgrrjlK_o5tpx4oAaXBeWCHH5RprI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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> ;
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}