@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI> .
@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:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_head {
  this: np:hasAssertion dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_assertion;
    np:hasProvenance dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_provenance;
    np:hasPublicationInfo dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_assertion a np:Assertion .
  
  dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_provenance a np:Provenance .
  
  dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_assertion {
  miriam-gene:3439 a ncit:C16612 .
  
  lld:C2711227 a ncit:C7057 .
  
  dgn-gda:DGN64e677e867ac2ce513e1ab45568685fa sio:SIO_000628 miriam-gene:3439, lld:C2711227;
    a sio:SIO_001121 .
}

dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_provenance {
  dgn-np:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_assertion dcterms:description
      "[Recent reports show that R70Q and L/C91M amino acid substitutions in the core from different hepatitis C virus (HCV) genotypes have been associated with variable responses to interferon (IFN) and ribavirin (RBV) therapy, as well to an increase of hepatocellular carcinoma (HCC) risk, liver steatosis and insulin resistance (IR).]. 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:22995142;
    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:NP227969.RAAINk5gU6walPnYZus9iR_1WGtNIUw5kqsypP9ONbcDI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
}