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- Bfd25d124a1f2cb94e0f8c2721d34b410 hasDbXref "NCIT:P378" @default.
- Bfd25d124a1f2cb94e0f8c2721d34b410 type Axiom @default.
- Bfd25d124a1f2cb94e0f8c2721d34b410 annotatedProperty IAO_0000115 @default.
- Bfd25d124a1f2cb94e0f8c2721d34b410 annotatedSource MONDO_0007656 @default.
- Bfd25d124a1f2cb94e0f8c2721d34b410 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.