@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q> .
@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:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_head {
  this: np:hasAssertion dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_assertion;
    np:hasProvenance dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_provenance;
    np:hasPublicationInfo dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_assertion a np:Assertion .
  
  dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_provenance a np:Provenance .
  
  dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNe7936f4c0bd74ad13af81e7736615d22 sio:SIO_000628 miriam-gene:1557, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_provenance {
  dgn-np:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_assertion dcterms:description
      "[We examined the contribution of CYP2C9 and CYP2C19 genotypes and drug interactions to the phenytoin metabolism among 97 Korean epileptic patients to determine if pharmacogenetic testing could be utilized in routine clinical practice.]. 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:17562299;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP682981.RAlnpBVoOcB-aLmw2-v_VSXEN9ccKgMHs8wIih-wD3e8Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}