@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM> .
@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:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_head {
  this: np:hasAssertion dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_assertion;
    np:hasProvenance dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_provenance;
    np:hasPublicationInfo dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_assertion a np:Assertion .
  
  dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_provenance a np:Provenance .
  
  dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C0013421 a ncit:C7057 .
  
  dgn-gda:DGNdc284d49a0a4c437c138278d1c3528da sio:SIO_000628 miriam-gene:1813, lld:C0013421;
    a sio:SIO_001121 .
}

dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_provenance {
  dgn-np:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_assertion dcterms:description
      "[Our findings are consistent with the theory of reduced dopamine D(2) receptor (D2R) availability in dystonia, although the possibility of increased endogenous dopamine, and consequently, competitive D2R occupancy cannot be ruled out.]. 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:18719906;
    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:NP288340.RAZwHdGnGLIuNfnWVTA0pVRN5c_ulPPoYbeRRjDDoDBYM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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: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" .
}