@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE> .
@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:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_head {
  this: np:hasAssertion dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion;
    np:hasProvenance dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_provenance;
    np:hasPublicationInfo dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion a np:Assertion .
  
  dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_provenance a np:Provenance .
  
  dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion {
  miriam-gene:120892 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN2051eb6f16f4ad3ed03562e6fbbd8dd3 sio:SIO_000628 miriam-gene:120892, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_provenance {
  dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion dcterms:description
      "[In light of recent findings about the wide role of LRRK2 under normal and pathological conditions, it is tempting to speculate that LRRK2 mutations might play an upstream influence on the etiology of not just PD but also several alpha-synuclein and tau pathologies, including AD.]. 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:19072560;
    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:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:40+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" .
}