@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_head {
  this: np:hasAssertion dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_assertion;
    np:hasProvenance dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_provenance;
    np:hasPublicationInfo dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_assertion a np:Assertion .
  
  dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_provenance a np:Provenance .
  
  dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_assertion {
  miriam-gene:282617 a ncit:C16612 .
  
  lld:C2825055 a ncit:C7057 .
  
  dgn-gda:DGN8af31829f5875a23e90e3351e09332f0 sio:SIO_000628 miriam-gene:282617, lld:C2825055;
    a sio:SIO_001122 .
}

dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_provenance {
  dgn-np:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_assertion dcterms:description
      "[In patients with recurrent HCV infection after orthotopic liver transplantation, combination analyses of single nucleotide polymorphisms of IL28B in recipient and donor tissues and mutations in HCV RNA allow prediction of SVR to PEG-IFN/RBV therapy.]. 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:20708617;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP145535.RAOxufg24teF_xRmeIJT7o3Gg0xEqusCZI1BfvpuW-xYE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:01+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}