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- NCIT_C84735 IAO_0000115 "A genetic metabolic disorder causing hypertrophic cardiomyopathy. Mutations of the LAMP2 gene have been reported in association with this disease." @default.
- NCIT_C84735 NCIT_NHC0 "C84735" @default.
- NCIT_C84735 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84735 NCIT_P108 "Glycogen Storage Disease Type IIb" @default.
- NCIT_C84735 NCIT_P207 "C0878677" @default.
- NCIT_C84735 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84735 NCIT_R176 NCIT_C116022 @default.
- NCIT_C84735 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84735 NCIT_R176 NCIT_C20194 @default.
- NCIT_C84735 normalizedInformationContent "100" @default.
- NCIT_C84735 referenceCount "1" @default.
- NCIT_C84735 hasExactSynonym "Danon Disease" @default.
- NCIT_C84735 hasExactSynonym "Glycogen Storage Disease Type IIb" @default.
- NCIT_C84735 inSubset NCIT_C165258 @default.
- NCIT_C84735 inSubset NCIT_C192842 @default.
- NCIT_C84735 type Class @default.
- NCIT_C84735 isDefinedBy ncit.owl @default.
- NCIT_C84735 label "Glycogen Storage Disease Type IIb" @default.
- NCIT_C84735 subClassOf B2278880f5bc1bf4511f2c43cf23ed8a7 @default.
- NCIT_C84735 subClassOf B682c8f56b7a6a74c3e046918993f9260 @default.
- NCIT_C84735 subClassOf NCIT_C2991 @default.
- NCIT_C84735 subClassOf NCIT_C3235 @default.
- NCIT_C84735 subClassOf NCIT_C34816 @default.
- NCIT_C84735 subClassOf NCIT_C4873 @default.
- NCIT_C84735 subClassOf NCIT_C53529 @default.
- NCIT_C84735 subClassOf NCIT_C53543 @default.
- NCIT_C84735 subClassOf NCIT_C53547 @default.
- NCIT_C84735 subClassOf NCIT_C61272 @default.
- NCIT_C84735 subClassOf NCIT_C7057 @default.
- NCIT_C84735 subClassOf NCIT_C84734 @default.
- NCIT_C84735 subClassOf NCIT_C84735 @default.