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- NCIT_C157123 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the STAT3 gene, encoding signal transducer and activator of transcription 3. It is characterized by variable features along a spectrum of autoimmune disorders affecting multiple organs. Common manifestations may include insulin-dependent diabetes mellitus and autoimmune enteropathy, or celiac disease, and autoimmune hematologic disorders. Other features include short stature and nonspecific dermatitis." @default.
- NCIT_C157123 NCIT_NHC0 "C157123" @default.
- NCIT_C157123 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C157123 NCIT_P108 "Infantile-Onset Multisystem Autoimmune Disease 1" @default.
- NCIT_C157123 NCIT_P208 "CL583648" @default.
- NCIT_C157123 NCIT_P322 "Cellosaurus" @default.
- NCIT_C157123 NCIT_R176 NCIT_C16612 @default.
- NCIT_C157123 NCIT_R176 NCIT_C20673 @default.
- NCIT_C157123 NCIT_R176 NCIT_C20710 @default.
- NCIT_C157123 NCIT_R176 NCIT_C24833 @default.
- NCIT_C157123 NCIT_R176 NCIT_C25991 @default.
- NCIT_C157123 NCIT_R176 NCIT_C54362 @default.
- NCIT_C157123 normalizedInformationContent "100" @default.
- NCIT_C157123 referenceCount "1" @default.
- NCIT_C157123 hasExactSynonym "ADMIO1" @default.
- NCIT_C157123 hasExactSynonym "Infantile-Onset Multisystem Autoimmune Disease 1" @default.
- NCIT_C157123 inSubset NCIT_C165258 @default.
- NCIT_C157123 inSubset NCIT_C192842 @default.
- NCIT_C157123 type Class @default.
- NCIT_C157123 isDefinedBy ncit.owl @default.
- NCIT_C157123 label "Infantile-Onset Multisystem Autoimmune Disease 1" @default.
- NCIT_C157123 subClassOf B6eda194f63db3b9901e83fafaa670392 @default.
- NCIT_C157123 subClassOf Bb8fc572fad0d219d8e09b5f676149dbe @default.
- NCIT_C157123 subClassOf NCIT_C157123 @default.
- NCIT_C157123 subClassOf NCIT_C2991 @default.
- NCIT_C157123 subClassOf NCIT_C4873 @default.
- NCIT_C157123 subClassOf NCIT_C53529 @default.
- NCIT_C157123 subClassOf NCIT_C53543 @default.
- NCIT_C157123 subClassOf NCIT_C53547 @default.
- NCIT_C157123 subClassOf NCIT_C7057 @default.