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- B0b7f5fa4d791da75bbb304bf63e737f9 NCIT_P378 "NCI" @default.
- B0b7f5fa4d791da75bbb304bf63e737f9 type Axiom @default.
- B0b7f5fa4d791da75bbb304bf63e737f9 annotatedProperty IAO_0000115 @default.
- B0b7f5fa4d791da75bbb304bf63e737f9 annotatedSource NCIT_C84727 @default.
- B0b7f5fa4d791da75bbb304bf63e737f9 annotatedTarget "A very rare and fatal disorder of spongiform encephalopathy usually caused by mutations of the prion protein (PRNP) gene. It is characterized by the accumulation of amyloid in the brain. Signs and symptoms include lack of motor coordination, unsteady gait, and difficulty walking. As the disease progresses, patients develop speech difficulties and dementia." @default.