@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k> .
@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:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_head {
  this: np:hasAssertion dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion ;
    np:hasProvenance dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_provenance ;
    np:hasPublicationInfo dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion a np:Assertion .
  dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_provenance a np:Provenance .
  dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  lld:C0152115 a ncit:C7057 .
  dgn-gda:DGN61486122be697454bb4426f021cd153b sio:SIO_000628 miriam-gene:6531 , lld:C0152115 ;
    a sio:SIO_001121 .
}
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_provenance {
  dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion dcterms:description "[We examined three polymorphisms in the dopamine D2 receptor gene (DRD2), two sites in the 3' region of the dopamine transporter (DAT) gene, two sites in the promoter and coding region of the dopamine D4 (DRD4) receptor gene, as well as polymorphic sites in the serotonin 6 receptor gene, the serotonin transporter gene and the tryptophan hydroxylase gene, for association with TD susceptibility.]. 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:14583797 ;
    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:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:34+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" .
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}