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- NCIT_C84545 IAO_0000115 "A rare genetic neurodegenerative disorder which belongs to the group of leukodystrophies. It has a slow and progressive clinical course and is characterized by developmental delay, macrocephaly, seizures, dementia and spasticity." @default.
- NCIT_C84545 NCIT_NHC0 "C84545" @default.
- NCIT_C84545 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84545 NCIT_P108 "Alexander Disease" @default.
- NCIT_C84545 NCIT_P207 "C0270726" @default.
- NCIT_C84545 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84545 NCIT_R100 NCIT_C12219 @default.
- NCIT_C84545 NCIT_R100 NCIT_C12755 @default.
- NCIT_C84545 NCIT_R100 NCIT_C12919 @default.
- NCIT_C84545 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84545 NCIT_R176 NCIT_C20744 @default.
- NCIT_C84545 NCIT_R176 NCIT_C20745 @default.
- NCIT_C84545 NCIT_R176 NCIT_C30073 @default.
- NCIT_C84545 NCIT_R176 NCIT_C68802 @default.
- NCIT_C84545 normalizedInformationContent "100" @default.
- NCIT_C84545 referenceCount "1" @default.
- NCIT_C84545 hasExactSynonym "Alexander Disease" @default.
- NCIT_C84545 inSubset NCIT_C165258 @default.
- NCIT_C84545 inSubset NCIT_C192842 @default.
- NCIT_C84545 type Class @default.
- NCIT_C84545 isDefinedBy ncit.owl @default.
- NCIT_C84545 label "Alexander Disease" @default.
- NCIT_C84545 subClassOf B35bfebbb69325a3399e04b12b33206dd @default.
- NCIT_C84545 subClassOf Bc24e61d68afb58aefea7277514bf4383 @default.
- NCIT_C84545 subClassOf NCIT_C26835 @default.
- NCIT_C84545 subClassOf NCIT_C27551 @default.
- NCIT_C84545 subClassOf NCIT_C27588 @default.
- NCIT_C84545 subClassOf NCIT_C2991 @default.
- NCIT_C84545 subClassOf NCIT_C4873 @default.
- NCIT_C84545 subClassOf NCIT_C53529 @default.
- NCIT_C84545 subClassOf NCIT_C53531 @default.
- NCIT_C84545 subClassOf NCIT_C53543 @default.
- NCIT_C84545 subClassOf NCIT_C53547 @default.
- NCIT_C84545 subClassOf NCIT_C61253 @default.
- NCIT_C84545 subClassOf NCIT_C7057 @default.
- NCIT_C84545 subClassOf NCIT_C84545 @default.