@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc> .
@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/v4.0.0/void/> .

dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_head {
  this: np:hasAssertion dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_assertion;
    np:hasProvenance dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_provenance;
    np:hasPublicationInfo dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_assertion a np:Assertion .
  
  dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_provenance a np:Provenance .
  
  dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN6a9574d904fd4a6dea8a581444b98591 sio:SIO_000628 miriam-gene:1565, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_provenance {
  dgn-np:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_assertion dcterms:description
      "[The frequencies of five mutations of the debrisoquine 4-hydroxylase (CYP2D6) gene (mutations D6-A, B, C, D, and T), corresponding to poor metabolizer (PM) phenotypes, were determined by restriction fragment length polymorphism (RFLP) and polymerase chain reaction (PCR) in 47 patients with Parkinson disease, and compared with the findings in 47 healthy controls.]. 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:8837703;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1358941.RA_oDvcFl_R-2JqbgrSEkpbHsD6JEAe3NKt81gZXAWlIc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:02+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}