@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE> .
@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:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_head {
  this: np:hasAssertion dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion ;
    np:hasProvenance dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_provenance ;
    np:hasPublicationInfo dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion a np:Assertion .
  dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_provenance a np:Provenance .
  dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion {
  miriam-gene:2030 a ncit:C16612 .
  lld:C0019196 a ncit:C7057 .
  dgn-gda:DGN92867a24a621f166452a836a66c071b1 sio:SIO_000628 miriam-gene:2030 , lld:C0019196 ;
    a sio:SIO_001121 .
}
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_provenance {
  dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion dcterms:description "[Patients (n=169) chronically infected with the hepatitis C virus genotype 1, treated with standard doses of pegylated interferon-α and weight-based doses of ribavirin for up to 48 weeks, were genotyped for 21 variants in nucleoside transporter genes SLC28A2, SLC28A3, SLC29A1, and SLC29A2, selected to include reported functional variants and to span the complete gene loci.]. 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:21346688 ;
    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:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:58+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" .
}