@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y> .
@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:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_head {
  this: np:hasAssertion dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion;
    np:hasProvenance dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_provenance;
    np:hasPublicationInfo dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion a np:Assertion .
  
  dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_provenance a np:Provenance .
  
  dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion {
  miriam-gene:120892 a ncit:C16612 .
  
  lld:C0752347 a ncit:C7057 .
  
  dgn-gda:DGN3873f35e863f3ff5dddab696f761756a sio:SIO_000628 miriam-gene:120892, lld:C0752347;
    a sio:SIO_001121 .
}

dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_provenance {
  dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion dcterms:description
      "[Neuropathology is characterized by loss of dopaminergic neurons in the substantia nigra pars compacta in all cases with accompanying Lewy pathology, or tau pathology or without intraneuronal inclusions, thus indicating that mutations in LRRK2 are not always manifested as Lewy body disease (LBD) or as alpha-synucleinopathy.]. 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:19142648;
    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:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:20+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" .
}