DOID:649

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • nervous system disease
              • central nervous system disease
                • brain disease
                  • prion disease
        • infectious disease
          • prion disease
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • prion disease ^xsd:string
• definition
  • A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins. ^xsd:string
    • dce:type
      • obo:ECO_0007637
      • obo:ECO_0007638
    • oio:hasDbXref
      • url:http://en.wikipedia.org/wiki/Prion ^xsd:string
      • url:http://www.cdc.gov/ncidod/dvrd/prions/ ^xsd:string
• has exact synonym
  • Spongiform Encephalopathy ^@en
  • Prion disease pathway ^@en
  • Prion protein disease ^@en
  • transmissible spongiform encephalopathy ^@en
  • prion induced disorder ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:649 ^xsd:string
• in_subset
  • obo:doid#DO_infectious_disease_slim
  • obo:doid#DO_FlyBase_slim
  • obo:doid#NCIthesaurus
• oio:hasDbXref
  • KEGG:05020 ^xsd:string
  • SNOMEDCT_US_2023_03_01:20484008 ^xsd:string
  • MESH:D017096 ^xsd:string
  • ICD10CM:A81.9 ^xsd:string
  • NCI:C128346 ^xsd:string
  • UMLS_CUI:C0162534 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • brain disease
  • infectious disease