@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w> .
@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/v3.0.0/void/> .

dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_head {
  this: np:hasAssertion dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_assertion;
    np:hasProvenance dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_provenance;
    np:hasPublicationInfo dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_assertion a np:Assertion .
  
  dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_provenance a np:Provenance .
  
  dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  
  lld:C0234133 a ncit:C7057 .
  
  dgn-gda:DGN08e1f441b82b5134fd9998ed820caf43 sio:SIO_000628 miriam-gene:6531, lld:C0234133;
    a sio:SIO_001122 .
}

dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_provenance {
  dgn-np:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_assertion dcterms:description
      "[There was no statistically significant association between genotype and allele frequencies of DRD2, SLC6A3, or COMT polymorphisms and the development of particular EPSs.In conclusion, the results of the present study showed for the first time the association between acute haloperidol-induced EPSs and SLC6A3 VNTR and COMT Val158Met polymorphisms.]. 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:23963056;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP698437.RAv71-ppZ3-8JNfmgjWIhqiedSrXGjF-sHlXtnai4hs2w130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:41+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}