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- Bd73873303728f7ed7925f6055a9e88a5 NCIT_P378 "NCI" @default.
- Bd73873303728f7ed7925f6055a9e88a5 type Axiom @default.
- Bd73873303728f7ed7925f6055a9e88a5 annotatedProperty IAO_0000115 @default.
- Bd73873303728f7ed7925f6055a9e88a5 annotatedSource NCIT_C84711 @default.
- Bd73873303728f7ed7925f6055a9e88a5 annotatedTarget "A very rare autosomal dominant inherited sleep disorder caused by a mutation in the gene responsible for the prion protein. It affects individuals usually in their fourth decade. Its initial manifestation is difficulty in falling asleep. It is followed by complete inability to sleep. Patients develop deterioration of their mental and motor functions and die soon after the first symptoms appear, because of the total absence of sleep." @default.