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- NCIT_C84711 IAO_0000115 "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.
- NCIT_C84711 NCIT_NHC0 "C84711" @default.
- NCIT_C84711 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84711 NCIT_P108 "Fatal Familial Insomnia" @default.
- NCIT_C84711 NCIT_P207 "C0206042" @default.
- NCIT_C84711 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84711 NCIT_R176 NCIT_C20194 @default.
- NCIT_C84711 NCIT_R176 NCIT_C71442 @default.
- NCIT_C84711 normalizedInformationContent "100" @default.
- NCIT_C84711 referenceCount "1" @default.
- NCIT_C84711 hasExactSynonym "Fatal Familial Insomnia" @default.
- NCIT_C84711 type Class @default.
- NCIT_C84711 isDefinedBy ncit.owl @default.
- NCIT_C84711 label "Fatal Familial Insomnia" @default.
- NCIT_C84711 subClassOf B4e8d08f10c7303b600830d7ce750835c @default.
- NCIT_C84711 subClassOf Bdc52cfce541704f2d0aee0e81512be5d @default.
- NCIT_C84711 subClassOf NCIT_C28286 @default.
- NCIT_C84711 subClassOf NCIT_C2893 @default.
- NCIT_C84711 subClassOf NCIT_C2991 @default.
- NCIT_C84711 subClassOf NCIT_C3376 @default.
- NCIT_C84711 subClassOf NCIT_C4873 @default.
- NCIT_C84711 subClassOf NCIT_C53529 @default.
- NCIT_C84711 subClassOf NCIT_C53543 @default.
- NCIT_C84711 subClassOf NCIT_C53547 @default.
- NCIT_C84711 subClassOf NCIT_C7057 @default.
- NCIT_C84711 subClassOf NCIT_C84711 @default.