@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A> .
@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:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_head {
  this: np:hasAssertion dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_assertion;
    np:hasProvenance dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_provenance;
    np:hasPublicationInfo dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_assertion a np:Assertion .
  
  dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_provenance a np:Provenance .
  
  dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_assertion {
  miriam-gene:6281 a ncit:C16612 .
  
  lld:C0333463 a ncit:C7057 .
  
  dgn-gda:DGNe55bfe5823b5909c36cd711afa77e1b0 sio:SIO_000628 miriam-gene:6281, lld:C0333463;
    a sio:SIO_001121 .
}

dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_provenance {
  dgn-np:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_assertion dcterms:description
      "[Neuropathology shows diffuse cerebral atrophy with neurofibrillary tangles, often ghost tangles, and neuropil threads almost limited to limbic areas (transentorhinal, entorhinal area, hippocampuS--not exclusively sector CA 1--and amygdala) with only rare and mild involvement of the neocortex, basal ganglia and brainstem (except nucleus basalis and locus ceruleus), absence of neuritic plaques and absence or scarcety of amyloid deposits.]. 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:9546293;
    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:NP495599.RAZztsUCXMWETsBgsKuJlt-Pgeyk3ChZdHv-ELm9L5B1A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}