@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE> .
@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:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_head {
  this: np:hasAssertion dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion;
    np:hasProvenance dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_provenance;
    np:hasPublicationInfo dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion a np:Assertion .
  
  dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_provenance a np:Provenance .
  
  dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion {
  miriam-gene:5071 a ncit:C16612 .
  
  lld:C0013384 a ncit:C7057 .
  
  dgn-gda:DGNfd4f6cfa83fcb3bb9ad059623973141f sio:SIO_000628 miriam-gene:5071, lld:C0013384;
    a sio:SIO_001121 .
}

dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_provenance {
  dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion dcterms:description
      "[None of them displayed any of the clinical hallmarks described in patients with previously reported parkin mutations, including diurnal fluctuations, benefit from sleep, foot dystonia, hyperreflexia, and early susceptibility to levodopa-induced dyskinesias.]. 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:10894217;
    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:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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" .
}