Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf97e1ab5874fe287bbbdb094ea08056c> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bf97e1ab5874fe287bbbdb094ea08056c NCIT_P378 "NCI" @default.
- Bf97e1ab5874fe287bbbdb094ea08056c type Axiom @default.
- Bf97e1ab5874fe287bbbdb094ea08056c annotatedProperty IAO_0000115 @default.
- Bf97e1ab5874fe287bbbdb094ea08056c annotatedSource NCIT_C26802 @default.
- Bf97e1ab5874fe287bbbdb094ea08056c 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.