@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc> .
@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:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_head {
  this: np:hasAssertion dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_assertion;
    np:hasProvenance dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_provenance;
    np:hasPublicationInfo dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_assertion a np:Assertion .
  
  dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_provenance a np:Provenance .
  
  dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_assertion {
  miriam-gene:1577 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGNa0ca008ddf3d01c5bb025d0a2cf5ce4a sio:SIO_000628 miriam-gene:1577, lld:C0023418;
    a sio:SIO_001122 .
}

dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_provenance {
  dgn-np:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_assertion dcterms:description
      "[The UGT1A1 6/6 genotype predicted lower catechol AUC. Prednisone strongly induces etoposide clearance, genetic polymorphisms may predict the constitutive and induced clearance of etoposide, and the relationship between genotype and phenotype differs by race.]. 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:12969965;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP60146.RAVTvG1dfWWPkLPIMr3kbvBiNuNwzXwhowUuh8nAiRJtc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}