@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI> .
@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:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_head {
   this: np:hasAssertion dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_assertion ;
    np:hasProvenance dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_provenance ;
    np:hasPublicationInfo dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_assertion a np:Assertion .
  dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_provenance a np:Provenance .
  dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_assertion {
   miriam-gene:54577 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
  dgn-gda:DGN40d3427b06aba5e1a21be8b479545678 sio:SIO_000628 miriam-gene:54577 , lld:C2239176 ;
    a sio:SIO_001121 .
}
dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_provenance {
   dgn-np:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_assertion dcterms:description "[In this study, we investigated the association between haplotypes of the whole UGT1A7 gene and the risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B. Sequence analysis of exon1 and the promoter region of the UGT1A7 gene was carried out to determine haplotype profiles for 244 patients with hepatocellular carcinoma, 223 hepatitis B carriers, and 314 healthy control subjects.]. 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:18271934 ;
    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:NP597091.RAGbIhd8tg1V4G4JiYt1q7xqkmSQJMnV47iaCTa8_wMtI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:59+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" .
}