@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg> .
@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 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:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_head {
  this: np:hasAssertion dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion;
    np:hasProvenance dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_provenance;
    np:hasPublicationInfo dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion a np:Assertion .
  
  dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_provenance a np:Provenance .
  
  dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNd0ca7834d3465cf7a71bafdd3ed701fc sio:SIO_000628 miriam-gene:1565, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_provenance {
  dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion dct:description
      "[A CYP2D6 phenotype-genotype mismatch (phenocopying) can occur in Japanese psychiatric patients receiving clinical doses of some psychotropic drugs where the prevalence of PMs is low and the pharmacodynamic responses to those drugs are enhanced compared to Caucasian patients.]. 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:14571354;
    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:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}