@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc> .
@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:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_head {
  this: np:hasAssertion dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_assertion;
    np:hasProvenance dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_provenance;
    np:hasPublicationInfo dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_assertion a np:Assertion .
  
  dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_provenance a np:Provenance .
  
  dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_assertion {
  miriam-gene:65018 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGN1014d5007b45f461cc063d48afe60776 sio:SIO_000628 miriam-gene:65018, lld:C0242422;
    a sio:SIO_001122 .
}

dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_provenance {
  dgn-np:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_assertion dcterms:description
      "[Since the substantia nigra plays an important role in temporal processing of sensory stimuli, as revealed from studies in idiopathic PD, we sought to investigate whether any subclinical sensory abnormalities could be detected in patients with PINK1- related parkinsonism and in unaffected PINK1 heterozygous carriers.]. 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:18584234;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP79292.RAKHIuGRjlev4izURCg3qCfrlIv1FxHAz7AMai54ZOhhc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:39+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" .
}