@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs> .
@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:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_head {
  this: np:hasAssertion dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_assertion;
    np:hasProvenance dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_provenance;
    np:hasPublicationInfo dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_assertion a np:Assertion .
  
  dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_provenance a np:Provenance .
  
  dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_assertion {
  miriam-gene:7054 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNc161079d1e2d7a0cecf082ab5d69ad5f sio:SIO_000628 miriam-gene:7054, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_provenance {
  dgn-np:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_assertion dcterms:description
      "[These findings on DRD indicate that the nigrostriatal DA neurons may be most susceptible to the decreases in GCH1 activity, BH4 level, TH activity, and DA level, and that DRD is the DA deficiency without neuronal death in contrast to juvenile parkinsonism or Parkinson's disease with DA cell death.]. 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:10661862;
    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:NP256489.RADu19M00aoR_f_PNrLG4yUCJVorfzPs-Fn7ne_Md1ABs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}