@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA> .
@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:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_head {
  this: np:hasAssertion dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_assertion;
    np:hasProvenance dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_provenance;
    np:hasPublicationInfo dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_assertion a np:Assertion .
  
  dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_provenance a np:Provenance .
  
  dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0021122 a ncit:C7057 .
  
  dgn-gda:DGNded6e928d6c2ba59f928975f80d6bee1 sio:SIO_000628 miriam-gene:1312, lld:C0021122;
    a sio:SIO_001121 .
}

dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_provenance {
  dgn-np:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_assertion dcterms:description
      "[Recent genetic studies have investigated associations between ICD and polymorphisms of genes involved in the dopamine metabolism pathway (COMT, DAT), dopamine receptors (DRD1, DRD2, DRD3, DRD4), serotonin receptors and its transporter (HTR2A, 5HTT), and glutamate receptors (GRIN2B).]. 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:23232665;
    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:NP321619.RAREw8hhL2fA9PxRhNsWUlE13rAYZCXhhZCIPA-pbbLCA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:44+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" .
}