@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI> .
@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:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_head {
  this: np:hasAssertion dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_assertion;
    np:hasProvenance dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_provenance;
    np:hasPublicationInfo dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_assertion a np:Assertion .
  
  dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_provenance a np:Provenance .
  
  dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_assertion {
  miriam-gene:6620 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN411ed3bb2318acf9d277e07ef7748679 sio:SIO_000628 miriam-gene:6620, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_provenance {
  dgn-np:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_assertion dcterms:description
      "[A drastic diminution of β-synuclein expression was observed in cortical areas of all samples that presented neuropathological features corresponding to pure diffuse Lewy body pathology and the clinical phenotype of dementia with Lewy bodies, but not in those with neuropathological features corresponding to diffuse Lewy body pathology and concomitant Alzheimer's disease pathology or the clinical phenotype of Parkinson's disease with dementia.]. 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:20959308;
    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:NP691546.RACTkc_cHa1pcvHIkJPK9D-OXKiK1Dh2evvX9IQaaVNKI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}