@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ> .
@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:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_head {
  this: np:hasAssertion dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion;
    np:hasProvenance dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion a np:Assertion .
  
  dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_provenance a np:Provenance .
  
  dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion {
  miriam-gene:6571 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN9babb723d2bdd8a8a5fa8cb6b7c48e12 sio:SIO_000628 miriam-gene:6571, lld:C0030567;
    a sio:SIO_001123 .
}

dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_provenance {
  dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion dcterms:description
      "[Low expression of VMAT2 in the substantia nigra of Parkinson's disease, the involvement of VMAT2 in Lewy body of the substantia nigra suggests the association of this protein in the neurodegeneration of nigral neurons in Parkinson's 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:16386370;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:08+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" .
}