@prefix nalt: <https://lod.nal.usda.gov/nalt/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix ns0: <https://lod.nal.usda.gov/naltv#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .

nalt:18995
  skos:prefLabel "enfermedades por prión"@es, "prion diseases"@en ;
  a <https://lod.nal.usda.gov/naltv#Topic>, skos:Concept ;
  skos:narrower nalt:18996 .

nalt:18996
  skos:altLabel "Creutzfeldt-Jakob Disease"@en, "new variant Creutzfeldt-Jakob Disease"@en, "Jakob-Creutzfeldt Syndrome"@en, "Jakob Creutzfeldt Disease"@en, "new variant Creutzfeldt-Jakob Syndrome"@en, "new variant Jakob Creutzfeldt Disease"@en, "V-CJD (Variant-Creutzfeldt-Jakob Disease)"@en, "Variant Creutzfeldt-Jakob Disease"@en, "Jakob-Creutzfeldt Disease"@en, "Creutzfeldt Jakob Syndrome"@en, "Jakob Creutzfeldt Syndrome"@en, "CJD (Creutzfeldt-Jakob Disease)"@en ;
  dc:modified "2012-11-30"^^xsd:date ;
  ns0:marc001 "10172" ;
  skos:prefLabel "Creutzfeldt-Jakob Syndrome"@en, "síndrome de Creutzfeldt-Jakob"@es ;
  skos:broader nalt:18995 ;
  skos:hiddenLabel "Creutzfeld-Jakob disease"@en, "Creutzfeldt-Jakob-Syndrome"@en, "Cruetzfeldt Jakob Disease"@en, "Creutzfeld-Jacob disease"@en, "Cruetzfeldt-Jakob Disease"@en ;
  skos:definition nalt:18996_def ;
  a ns0:Topic, skos:Concept ;
  skos:inScheme <https://lod.nal.usda.gov/nalt> ;
  skos:related nalt:18992 ;
  dc:created "2006-01-19"^^xsd:date .

ns0:Topic
  rdfs:label "Topic"@en ;
  a owl:Class .

<https://lod.nal.usda.gov/nalt>
  rdfs:label "NALT Full"@en ;
  a skos:ConceptScheme .

nalt:18996_def
  rdf:value "Encefalopatía transmisible de ocurrencia rara, prevalente entre las edades de 50 y 70 años. Los individuos afectados pueden presentar alteraciones del sueño, cambios de personalidad, ataxia, afasia, pérdida de visión, debilidad, atrofia muscular, mioclonia, demencia progresiva, y muerte dentro de un año de iniciada la enfermedad. Entre las características patológicas se incluye una degeneración espongiforme cerebrocortical y cerebelar prominente y la presencia de priones."@es, "A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ataxia, aphasia, visual loss, weakness, muscle atrophy, myoclonus, progressive dementia, and death within one year of disease onset. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of prions."@en ;
  dc:source "NAL Thesaurus Staff" ;
  a ns0:Definition .

nalt:18992
  skos:prefLabel "encefalopatía espongiforme bovina"@es, "bovine spongiform encephalopathy"@en ;
  a ns0:Topic, skos:Concept ;
  skos:related nalt:18996 .