@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA> .
@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:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_head {
  this: np:hasAssertion dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_assertion;
    np:hasProvenance dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_provenance;
    np:hasPublicationInfo dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_assertion a np:Assertion .
  
  dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_provenance a np:Provenance .
  
  dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_assertion {
  miriam-gene:1576 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNa3285f6022f078d3e22aa3c34473da8e sio:SIO_000628 miriam-gene:1576, lld:C0006826;
    a sio:SIO_001122 .
}

dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_provenance {
  dgn-np:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_assertion dcterms:description
      "[When compared with healthy Chinese population data, the 6beta-hydroxycortisol to free cortisol ratio data suggested that these alleles (CYP3A4*4, CYP3A4*5, and CYP3A4*6) may decrease the CYP3A4 activity. Incidences of these mutations in Chinese subjects are rare. The prevalence of these point mutations in other ethnic groups and its effect on the metabolic activity of CYP3A4 remain to be further evaluated.]. 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:11181494;
    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:NP60083.RARJDxFdHUkcbGSb53x8nhe-9-aPUFF6xV9Rb7BOuWmHA130_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" .
}