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- NCIT_C153290 IAO_0000115 "The most common form of Rubinstein-Taybi syndrome, caused by a mutation in the CREB binding protein (CREBBP) gene." @default.
- NCIT_C153290 NCIT_A13 NCIT_C26568 @default.
- NCIT_C153290 NCIT_NHC0 "C153290" @default.
- NCIT_C153290 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C153290 NCIT_P108 "Rubinstein-Taybi Syndrome Type 1" @default.
- NCIT_C153290 NCIT_P208 "CL554407" @default.
- NCIT_C153290 NCIT_P322 "Cellosaurus" @default.
- NCIT_C153290 NCIT_R176 NCIT_C16612 @default.
- NCIT_C153290 NCIT_R176 NCIT_C21281 @default.
- NCIT_C153290 NCIT_R176 NCIT_C25870 @default.
- NCIT_C153290 NCIT_R176 NCIT_C26568 @default.
- NCIT_C153290 normalizedInformationContent "100" @default.
- NCIT_C153290 referenceCount "1" @default.
- NCIT_C153290 hasExactSynonym "RSTS1" @default.
- NCIT_C153290 hasExactSynonym "Rubinstein-Taybi Syndrome Type 1" @default.
- NCIT_C153290 inSubset NCIT_C165258 @default.
- NCIT_C153290 inSubset NCIT_C192842 @default.
- NCIT_C153290 type Class @default.
- NCIT_C153290 isDefinedBy ncit.owl @default.
- NCIT_C153290 label "Rubinstein-Taybi Syndrome Type 1" @default.
- NCIT_C153290 subClassOf B9d99dc292e2685cb11bd7f53ce2c0224 @default.
- NCIT_C153290 subClassOf Bdc42efdb4a326bf52250afc3930269c0 @default.
- NCIT_C153290 subClassOf NCIT_C153290 @default.
- NCIT_C153290 subClassOf NCIT_C28193 @default.
- NCIT_C153290 subClassOf NCIT_C2991 @default.
- NCIT_C153290 subClassOf NCIT_C35561 @default.
- NCIT_C153290 subClassOf NCIT_C4873 @default.
- NCIT_C153290 subClassOf NCIT_C54705 @default.
- NCIT_C153290 subClassOf NCIT_C7057 @default.
- NCIT_C153290 subClassOf NCIT_C75466 @default.