@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A> .
@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:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_head {
  this: np:hasAssertion dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_assertion;
    np:hasProvenance dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_provenance;
    np:hasPublicationInfo dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_assertion a np:Assertion .
  
  dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_provenance a np:Provenance .
  
  dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_assertion {
  miriam-gene:2675 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN6a801dc6faaab4fefc6cb63c5bf27b17 sio:SIO_000628 miriam-gene:2675, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_provenance {
  dgn-np:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_assertion dcterms:description
      "[These results illustrate the combined use of genetic markers to predict enhanced response to iloperidone and support the application of pharmacogenetics to differentiate medication options and improve individualized treatments for 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:19573479;
    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:NP74528.RAXPYMOHAtQiPR_9jhP7uQxaGyBnm4VR-GSXTSKfyhc5A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}