@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM> .
@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:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_head {
  this: np:hasAssertion dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_assertion;
    np:hasProvenance dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_provenance;
    np:hasPublicationInfo dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_assertion a np:Assertion .
  
  dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_provenance a np:Provenance .
  
  dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_assertion {
  miriam-gene:55885 a ncit:C16612 .
  
  lld:C0004936 a ncit:C7057 .
  
  dgn-gda:DGN6202e9621c996d4de31bf3a804acaf35 sio:SIO_000628 miriam-gene:55885, lld:C0004936;
    a sio:SIO_001121 .
}

dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_provenance {
  dgn-np:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_assertion dcterms:description
      "[The dopamine transporter (DAT) is the site of action of stimulants, and variations in the human DAT gene (DAT1) have been associated with susceptibility to several psychiatric disorders including attention deficit hyperactivity disorder (ADHD) and bipolar disorder.]. 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:16261167;
    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:NP215170.RA60Jo_br0shKCK5B7tvgoFMEuKVfs3i2cUxIUq7962fM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:59+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" .
}