@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo> .
@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:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_head {
  this: np:hasAssertion dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion;
    np:hasProvenance dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_provenance;
    np:hasPublicationInfo dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion a np:Assertion .
  
  dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_provenance a np:Provenance .
  
  dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion {
  miriam-gene:283871 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN4483a1460fae77a1e681180f60a2302f sio:SIO_000628 miriam-gene:283871, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_provenance {
  dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion dcterms:description
      "[The analysis using C1236T or G2677AT genotypes gave similar results, due to linkage of these polymorphisms.PGP polymorphisms may affect the penetration of olanzapine into the central nervous system as seen by a relationship between the 3435T allele, olanzapine plasma levels, and reduction in the positive symptoms of schizophrenia.]. 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:17038883;
    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:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}