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- NCIT_C61258 IAO_0000115 "A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments." @default.
- NCIT_C61258 NCIT_NHC0 "C61258" @default.
- NCIT_C61258 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C61258 NCIT_P108 "Neuronal Ceroid Lipofuscinosis Type 3" @default.
- NCIT_C61258 NCIT_P207 "C0751383" @default.
- NCIT_C61258 NCIT_P322 "Cellosaurus" @default.
- NCIT_C61258 NCIT_P366 "Batten_Disease" @default.
- NCIT_C61258 NCIT_R176 NCIT_C156970 @default.
- NCIT_C61258 NCIT_R176 NCIT_C16612 @default.
- NCIT_C61258 NCIT_R176 NCIT_C21295 @default.
- NCIT_C61258 NCIT_R176 NCIT_C26006 @default.
- NCIT_C61258 NCIT_R176 NCIT_C28533 @default.
- NCIT_C61258 normalizedInformationContent "100" @default.
- NCIT_C61258 referenceCount "1" @default.
- NCIT_C61258 hasExactSynonym "Batten Disease" @default.
- NCIT_C61258 hasExactSynonym "CLN3" @default.
- NCIT_C61258 hasExactSynonym "Neuronal Ceroid Lipofuscinosis Type 3" @default.
- NCIT_C61258 inSubset NCIT_C165258 @default.
- NCIT_C61258 inSubset NCIT_C192842 @default.
- NCIT_C61258 type Class @default.
- NCIT_C61258 isDefinedBy ncit.owl @default.
- NCIT_C61258 label "Neuronal Ceroid Lipofuscinosis Type 3" @default.
- NCIT_C61258 subClassOf B2c8f545919e616028179bd6d97eee422 @default.
- NCIT_C61258 subClassOf Bd6ceea19d28d4a65489c3cc15c86537f @default.
- NCIT_C61258 subClassOf NCIT_C2991 @default.
- NCIT_C61258 subClassOf NCIT_C3235 @default.
- NCIT_C61258 subClassOf NCIT_C34816 @default.
- NCIT_C61258 subClassOf NCIT_C53529 @default.
- NCIT_C61258 subClassOf NCIT_C53547 @default.
- NCIT_C61258 subClassOf NCIT_C61257 @default.
- NCIT_C61258 subClassOf NCIT_C61258 @default.
- NCIT_C61258 subClassOf NCIT_C7057 @default.