@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8> .
@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:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_head {
  this: np:hasAssertion dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_assertion;
    np:hasProvenance dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_provenance;
    np:hasPublicationInfo dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_assertion a np:Assertion .
  
  dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_provenance a np:Provenance .
  
  dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_assertion {
  miriam-gene:54658 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN264d4438e86a9687f4c402d63ce7a7d9 sio:SIO_000628 miriam-gene:54658, lld:C0010068;
    a sio:SIO_001122 .
}

dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_provenance {
  dgn-np:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_assertion dcterms:description
      "[Although the concentration of bilirubin in the UGT1A1 variant is higher than the wild type for the patients with coronary disease (CAD), there is no significant difference in the polymorphism between the patients and the participants in the control group.]. 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:17952380;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:08+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" .
}