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- NCIT_C188214 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the GRN gene, encoding progranulin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments." @default.
- NCIT_C188214 NCIT_NHC0 "C188214" @default.
- NCIT_C188214 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C188214 NCIT_P108 "Neuronal Ceroid Lipofuscinosis Type 11" @default.
- NCIT_C188214 NCIT_P208 "CL1793115" @default.
- NCIT_C188214 NCIT_P322 "Cellosaurus" @default.
- NCIT_C188214 NCIT_R176 NCIT_C101401 @default.
- NCIT_C188214 NCIT_R176 NCIT_C16612 @default.
- NCIT_C188214 NCIT_R176 NCIT_C21550 @default.
- NCIT_C188214 normalizedInformationContent "100" @default.
- NCIT_C188214 referenceCount "1" @default.
- NCIT_C188214 hasExactSynonym "CLN11" @default.
- NCIT_C188214 hasExactSynonym "Neuronal Ceroid Lipofuscinosis Type 11" @default.
- NCIT_C188214 inSubset NCIT_C165258 @default.
- NCIT_C188214 inSubset NCIT_C192842 @default.
- NCIT_C188214 type Class @default.
- NCIT_C188214 isDefinedBy ncit.owl @default.
- NCIT_C188214 label "Neuronal Ceroid Lipofuscinosis Type 11" @default.
- NCIT_C188214 subClassOf B25def1681f1d0c19f380e5b23bb2234b @default.
- NCIT_C188214 subClassOf Bc06e45adf8792720358f71a715f0dbf3 @default.
- NCIT_C188214 subClassOf NCIT_C188214 @default.
- NCIT_C188214 subClassOf NCIT_C2991 @default.
- NCIT_C188214 subClassOf NCIT_C3235 @default.
- NCIT_C188214 subClassOf NCIT_C34816 @default.
- NCIT_C188214 subClassOf NCIT_C53529 @default.
- NCIT_C188214 subClassOf NCIT_C53547 @default.
- NCIT_C188214 subClassOf NCIT_C61257 @default.
- NCIT_C188214 subClassOf NCIT_C7057 @default.