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- NCIT_C157150 IAO_0000115 "An autosomal recessive subtype of hereditary spastic paraplegia caused by mutation(s) in the CAPN1 gene, encoding calpain-1 catalytic subunit." @default.
- NCIT_C157150 NCIT_NHC0 "C157150" @default.
- NCIT_C157150 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C157150 NCIT_P108 "Spastic Paraplegia 76" @default.
- NCIT_C157150 NCIT_P208 "CL936904" @default.
- NCIT_C157150 NCIT_P322 "Cellosaurus" @default.
- NCIT_C157150 NCIT_R100 NCIT_C12219 @default.
- NCIT_C157150 NCIT_R100 NCIT_C12438 @default.
- NCIT_C157150 NCIT_R100 NCIT_C12755 @default.
- NCIT_C157150 NCIT_R100 NCIT_C12919 @default.
- NCIT_C157150 NCIT_R100 NCIT_C13040 @default.
- NCIT_C157150 NCIT_R100 NCIT_C32221 @default.
- NCIT_C157150 NCIT_R176 NCIT_C123832 @default.
- NCIT_C157150 NCIT_R176 NCIT_C16612 @default.
- NCIT_C157150 NCIT_R176 NCIT_C21281 @default.
- NCIT_C157150 NCIT_R176 NCIT_C25804 @default.
- NCIT_C157150 NCIT_R176 NCIT_C26003 @default.
- NCIT_C157150 NCIT_R176 NCIT_C28404 @default.
- NCIT_C157150 normalizedInformationContent "100" @default.
- NCIT_C157150 referenceCount "1" @default.
- NCIT_C157150 hasExactSynonym "Spastic Paraplegia 76" @default.
- NCIT_C157150 inSubset NCIT_C165258 @default.
- NCIT_C157150 inSubset NCIT_C192842 @default.
- NCIT_C157150 type Class @default.
- NCIT_C157150 isDefinedBy ncit.owl @default.
- NCIT_C157150 label "Spastic Paraplegia 76" @default.
- NCIT_C157150 subClassOf B6de9650e47c9663e1793a458fc868529 @default.
- NCIT_C157150 subClassOf B8a19f12fe32f8169cda929b2b46ee77e @default.
- NCIT_C157150 subClassOf NCIT_C140267 @default.
- NCIT_C157150 subClassOf NCIT_C157150 @default.
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- NCIT_C157150 subClassOf NCIT_C4802 @default.
- NCIT_C157150 subClassOf NCIT_C53529 @default.
- NCIT_C157150 subClassOf NCIT_C53531 @default.
- NCIT_C157150 subClassOf NCIT_C53547 @default.
- NCIT_C157150 subClassOf NCIT_C7057 @default.