@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic> .
@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:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_head {
  this: np:hasAssertion dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_assertion;
    np:hasProvenance dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_provenance;
    np:hasPublicationInfo dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_assertion a np:Assertion .
  
  dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_provenance a np:Provenance .
  
  dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_assertion {
  miriam-gene:282617 a ncit:C16612 .
  
  lld:C1623038 a ncit:C7057 .
  
  dgn-gda:DGNe328c821e112cc73717434bc7309a2a0 sio:SIO_000628 miriam-gene:282617, lld:C1623038;
    a sio:SIO_001121 .
}

dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_provenance {
  dgn-np:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_assertion dcterms:description
      "[IL-28B rs12979860 C/T polymorphism T allele is more prevalent in patients with viral cirrhosis due to HCV in comparison to other aetiologies and to patients with mild chronic hepatitis C. Among OLT patients, carriage of this allele seems to augment the risk of developing HCC.]. 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:21146242;
    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:NP889691.RA694tU15Gargessks2TAMMAFzVEeSUclLRgVKABag4ic130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:07+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" .
}