@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ> .
@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:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_head {
  this: np:hasAssertion dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_assertion;
    np:hasProvenance dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_provenance;
    np:hasPublicationInfo dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_assertion a np:Assertion .
  
  dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_provenance a np:Provenance .
  
  dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  
  lld:C0011570 a ncit:C7057 .
  
  dgn-gda:DGN6e962ba74da8df93811bfc00585bed7b sio:SIO_000628 miriam-gene:1557, lld:C0011570;
    a sio:SIO_001122 .
}

dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_provenance {
  dgn-np:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_assertion dcterms:description
      "[ Combined pharmacogenetic testing for CYP2D6 and CYP2C19 identifies patients with low risk for side effects in amitriptyline therapy and could possibly be used to individualize antidepressive regimens and reduce treatment cost. Identification of genotypes associated with slightly reduced intermediate metabolism may be more important than currently anticipated. It could also be the key to demonstrating cost-effectiveness for CYP2D6 genotyping in critical dose drugs.]. 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:15590749;
    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:NP45800.RAEZoeYIeiv2MBrolNG3arZv6Eh2DyB-2OF9rFiJR1RBQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}