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- NCIT_C176898 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the PMP22 gene, encoding peripheral myelin protein 22. Neuropathy is precipitated by mechanical compression on a nerve, typically with onset in the first and second decades." @default.
- NCIT_C176898 NCIT_NHC0 "C176898" @default.
- NCIT_C176898 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176898 NCIT_P108 "Neuropathy, Recurrent, with Pressure Palsies" @default.
- NCIT_C176898 NCIT_P207 "C0393814" @default.
- NCIT_C176898 NCIT_P322 "Cellosaurus" @default.
- NCIT_C176898 NCIT_R100 NCIT_C12219 @default.
- NCIT_C176898 NCIT_R100 NCIT_C12755 @default.
- NCIT_C176898 NCIT_R100 NCIT_C12919 @default.
- NCIT_C176898 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176898 NCIT_R176 NCIT_C20744 @default.
- NCIT_C176898 NCIT_R176 NCIT_C75900 @default.
- NCIT_C176898 normalizedInformationContent "100" @default.
- NCIT_C176898 referenceCount "1" @default.
- NCIT_C176898 hasExactSynonym "HNPP" @default.
- NCIT_C176898 hasExactSynonym "Hereditary Neuropathy with Liability to Pressure Palsies" @default.
- NCIT_C176898 hasExactSynonym "Neuropathy, Recurrent, with Pressure Palsies" @default.
- NCIT_C176898 inSubset NCIT_C165258 @default.
- NCIT_C176898 inSubset NCIT_C192842 @default.
- NCIT_C176898 type Class @default.
- NCIT_C176898 isDefinedBy ncit.owl @default.
- NCIT_C176898 label "Neuropathy, Recurrent, with Pressure Palsies" @default.
- NCIT_C176898 subClassOf B1053b2e37921e42127e7265502994de3 @default.
- NCIT_C176898 subClassOf Ba9057804a7cb9de6a919228332532f88 @default.
- NCIT_C176898 subClassOf NCIT_C176898 @default.
- NCIT_C176898 subClassOf NCIT_C26835 @default.
- NCIT_C176898 subClassOf NCIT_C27551 @default.
- NCIT_C176898 subClassOf NCIT_C2991 @default.
- NCIT_C176898 subClassOf NCIT_C4731 @default.
- NCIT_C176898 subClassOf NCIT_C7057 @default.