@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw> .
@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:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_head {
  this: np:hasAssertion dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion ;
    np:hasProvenance dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_provenance ;
    np:hasPublicationInfo dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion a np:Assertion .
  dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_provenance a np:Provenance .
  dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGN0112d0747a3e7232f96a116f51219ab5 sio:SIO_000628 miriam-gene:1813 , lld:C0036341 ;
    a sio:SIO_001122 .
}
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_provenance {
  dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion dcterms:description "[We investigated 16 polymorphisms from three genes, dopamine receptor D2 (DRD2), catechol-O-methyl transferase (COMT) and brain derived neurotrophic factor (BDNF), which are involved in the dopaminergic pathways, and have been reported to be associated with susceptibility to schizophrenia and response to antipsychotic therapy.]. 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:19207030 ;
    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:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}