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- NCIT_C132196 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the CPN1 gene, encoding carboxypeptidase N catalytic chain. It may be characterized by episodic angioedema, chronic urticaria, asthma and/or allergic hypersensitivity." @default.
- NCIT_C132196 NCIT_NHC0 "C132196" @default.
- NCIT_C132196 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C132196 NCIT_P108 "Carboxypeptidase N Deficiency" @default.
- NCIT_C132196 NCIT_P207 "C0398782" @default.
- NCIT_C132196 NCIT_P322 "Cellosaurus" @default.
- NCIT_C132196 NCIT_R176 NCIT_C16612 @default.
- NCIT_C132196 NCIT_R176 NCIT_C178690 @default.
- NCIT_C132196 NCIT_R176 NCIT_C21275 @default.
- NCIT_C132196 NCIT_R176 NCIT_C21281 @default.
- NCIT_C132196 NCIT_R176 NCIT_C25804 @default.
- NCIT_C132196 NCIT_R176 NCIT_C26003 @default.
- NCIT_C132196 normalizedInformationContent "100" @default.
- NCIT_C132196 referenceCount "1" @default.
- NCIT_C132196 hasExactSynonym "Carboxypeptidase N Deficiency" @default.
- NCIT_C132196 inSubset NCIT_C165258 @default.
- NCIT_C132196 inSubset NCIT_C192842 @default.
- NCIT_C132196 type Class @default.
- NCIT_C132196 isDefinedBy ncit.owl @default.
- NCIT_C132196 label "Carboxypeptidase N Deficiency" @default.
- NCIT_C132196 subClassOf B7c711298ad0eb3d451c42fa8b6c503c4 @default.
- NCIT_C132196 subClassOf Bb4994e0b4927a819bdfae258da4b0896 @default.
- NCIT_C132196 subClassOf NCIT_C132196 @default.
- NCIT_C132196 subClassOf NCIT_C2991 @default.
- NCIT_C132196 subClassOf NCIT_C4873 @default.
- NCIT_C132196 subClassOf NCIT_C53529 @default.
- NCIT_C132196 subClassOf NCIT_C53543 @default.
- NCIT_C132196 subClassOf NCIT_C53547 @default.
- NCIT_C132196 subClassOf NCIT_C7057 @default.