@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA> .
@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:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_head {
  this: np:hasAssertion dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_assertion;
    np:hasProvenance dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_provenance;
    np:hasPublicationInfo dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_assertion a np:Assertion .
  
  dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_provenance a np:Provenance .
  
  dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN16ba292b48bc0c1d911d9167f76c9f9e sio:SIO_000628 miriam-gene:348, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_provenance {
  dgn-np:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_assertion dct:description
      "[To determine whether the frequency of dopamine receptor genetic variants and APOE alleles in patients with PD with and without chronic visual hallucinations resembles the pattern previously documented in patients with Alzheimer disease.]. 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:11176958;
    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:NP48208.RAjyhWhHy1L0BU-Ll8Ga6bCW-lYUGDiCkjU_rTB4FLaWA130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+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" .
}