@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y> .
@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 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:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_head {
  this: np:hasAssertion dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion ;
    np:hasProvenance dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion a np:Assertion .
  dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance a np:Provenance .
  dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion {
  miriam-gene:1815 a ncit:C16612 .
  lld:C0005586 a ncit:C7057 .
  dgn-gda:DGN2ff9b8f60b7df2c8a694ae994ceb99f7 sio:SIO_000628 miriam-gene:1815 , lld:C0005586 ;
    a sio:SIO_001122 .
}
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance {
  dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion dct:description "[ The results suggests that the studied gene variants of type D2 dopamine receptors are not promising candidate genes for bipolar affective illness. We did not consider the family history of the examined subjects, and also the control group was not psychiatrically screened, which may contribute to the lack of significant results.]. 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:15917720 ;
    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:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}