@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI> .
@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:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_head {
  this: np:hasAssertion dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_assertion ;
    np:hasProvenance dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_provenance ;
    np:hasPublicationInfo dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_assertion a np:Assertion .
  dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_provenance a np:Provenance .
  dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_assertion {
  miriam-gene:412 a ncit:C16612 .
  lld:C1623038 a ncit:C7057 .
  dgn-gda:DGN0bbac0a74bbc81fa6c4069777726a5fe sio:SIO_000628 miriam-gene:412 , lld:C1623038 ;
    a sio:SIO_001121 .
}
dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_provenance {
  dgn-np:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_assertion dcterms:description "[This study was performed to determine the distribution of hepatitis C virus (HCV) genotypes among asymptomatic carriers (ASC) and patients with chronic hepatitis without cirrhosis (NC-CH), liver cirrhosis (LC), and hepatocellular carcinoma (HCC) in the Osaka area, and to assess whether infection with HCV genotype 1b (II) is more likely to develop into hepatocellular carcinoma (HCC) than is that with genotype 2a (III) or genotype 2b (IV).]. 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:9816816 ;
    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:NP847195.RAO4f5qplm1Wo8KrGcnvTfEcSEWr2Kj6cD-fnpqNqoMTI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:38+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> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}