Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb29fdec845560032ebd3398589839f28> ?p ?o ?g. }
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- Bb29fdec845560032ebd3398589839f28 hasDbXref "NCIT:P378" @default.
- Bb29fdec845560032ebd3398589839f28 type Axiom @default.
- Bb29fdec845560032ebd3398589839f28 annotatedProperty IAO_0000115 @default.
- Bb29fdec845560032ebd3398589839f28 annotatedSource MONDO_0005357 @default.
- Bb29fdec845560032ebd3398589839f28 annotatedTarget "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.