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

<https://lod.nal.usda.gov/naltv#marc001> rdfs:label "Field 001 in MARC Authority Format"@en .
nalt:18996_def
  a <https://lod.nal.usda.gov/naltv#Definition> ;
  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" .

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

<https://lod.nal.usda.gov/naltv#Topic>
  a owl:Class ;
  rdfs:label "Topic"@en .

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

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

nalt:18995
  a ns0:Topic, skos:Concept ;
  skos:narrower nalt:18996 ;
  skos:prefLabel "enfermedades por prión"@es, "prion diseases"@en .