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- Bd6ee2f97a2fa73dd89fb5cac9b61782b hasDbXref "NCIT:P378" @default.
- Bd6ee2f97a2fa73dd89fb5cac9b61782b type Axiom @default.
- Bd6ee2f97a2fa73dd89fb5cac9b61782b annotatedProperty IAO_0000115 @default.
- Bd6ee2f97a2fa73dd89fb5cac9b61782b annotatedSource MONDO_0007656 @default.
- Bd6ee2f97a2fa73dd89fb5cac9b61782b 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.