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- NCIT_C26802 IAO_0000115 "A rare transmittable degenerative disorder of the brain caused by prions. Morphologically it is characterized by spongiform degeneration of the cerebral and cerebellar cortex. Signs and symptoms include sleep disturbances, personality changes, aphasia, ataxia, muscle atrophy and weakness, visual loss, and myoclonus. It usually leads to death within a year from the onset of the disease." @default.
- NCIT_C26802 NCIT_NHC0 "C26802" @default.
- NCIT_C26802 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C26802 NCIT_P108 "Creutzfeldt-Jakob Disease" @default.
- NCIT_C26802 NCIT_P207 "C0022336" @default.
- NCIT_C26802 NCIT_P322 "NICHD" @default.
- NCIT_C26802 NCIT_P325 "A prion disease of humans that is characterized by spongiform degeneration of the cerebral and cerebellar cortex. Three recognized forms are sporadic, familial, and iatrogenic. The iatrogenic form occurs through direct contact with human tissue, a product derived from human tissue, or contaminated medical equipment." @default.
- NCIT_C26802 NCIT_P366 "Creutzfeldt-Jacob_Disease" @default.
- NCIT_C26802 NCIT_R100 NCIT_C12219 @default.
- NCIT_C26802 NCIT_R100 NCIT_C12438 @default.
- NCIT_C26802 NCIT_R100 NCIT_C12755 @default.
- NCIT_C26802 NCIT_R100 NCIT_C12919 @default.
- NCIT_C26802 NCIT_R100 NCIT_C13040 @default.
- NCIT_C26802 NCIT_R100 NCIT_C32221 @default.
- NCIT_C26802 NCIT_R101 NCIT_C12219 @default.
- NCIT_C26802 NCIT_R101 NCIT_C12439 @default.
- NCIT_C26802 NCIT_R101 NCIT_C13018 @default.
- NCIT_C26802 NCIT_R101 NCIT_C13040 @default.
- NCIT_C26802 NCIT_R101 NCIT_C32221 @default.
- NCIT_C26802 NCIT_R101 NCIT_C33966 @default.
- NCIT_C26802 NCIT_R176 NCIT_C16612 @default.
- NCIT_C26802 NCIT_R176 NCIT_C20194 @default.
- NCIT_C26802 NCIT_R176 NCIT_C71442 @default.
- NCIT_C26802 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C26802 referenceCount "4" @default.
- NCIT_C26802 hasExactSynonym "CJD" @default.
- NCIT_C26802 hasExactSynonym "Classic Creutzfeldt-Jakob Disease" @default.
- NCIT_C26802 hasExactSynonym "Creutzfeldt-Jacob Disease" @default.
- NCIT_C26802 hasExactSynonym "Creutzfeldt-Jakob Disease" @default.
- NCIT_C26802 inSubset NCIT_C128453 @default.
- NCIT_C26802 inSubset NCIT_C90259 @default.
- NCIT_C26802 type Class @default.
- NCIT_C26802 isDefinedBy ncit.owl @default.
- NCIT_C26802 label "Creutzfeldt-Jakob Disease" @default.
- NCIT_C26802 subClassOf B1ab4a99d962808e2305d7a0422828a18 @default.
- NCIT_C26802 subClassOf Bd08fcd497c07081655b47d8667c20b00 @default.
- NCIT_C26802 subClassOf NCIT_C128346 @default.
- NCIT_C26802 subClassOf NCIT_C26726 @default.
- NCIT_C26802 subClassOf NCIT_C26802 @default.
- NCIT_C26802 subClassOf NCIT_C26835 @default.
- NCIT_C26802 subClassOf NCIT_C26920 @default.
- NCIT_C26802 subClassOf NCIT_C27551 @default.
- NCIT_C26802 subClassOf NCIT_C27582 @default.
- NCIT_C26802 subClassOf NCIT_C27583 @default.
- NCIT_C26802 subClassOf NCIT_C27586 @default.
- NCIT_C26802 subClassOf NCIT_C27588 @default.
- NCIT_C26802 subClassOf NCIT_C27590 @default.
- NCIT_C26802 subClassOf NCIT_C2934 @default.
- NCIT_C26802 subClassOf NCIT_C2991 @default.
- NCIT_C26802 subClassOf NCIT_C53529 @default.
- NCIT_C26802 subClassOf NCIT_C53531 @default.
- NCIT_C26802 subClassOf NCIT_C53547 @default.
- NCIT_C26802 subClassOf NCIT_C7057 @default.
- NCIT_C26802 subClassOf NCIT_C93210 @default.
- NCIT_C26802 subClassOf NCIT_C96413 @default.
- NCIT_C26802 subClassOf NCIT_C97154 @default.