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- NCIT_C176630 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the CARD11 gene, encoding caspase recruitment domain-containing protein 11. It is characterized by the onset of moderate to severe atopic dermatitis in early childhood, defects in T-cell activation, increased IgE, and eosinophilia." @default.
- NCIT_C176630 NCIT_A13 NCIT_C60668 @default.
- NCIT_C176630 NCIT_NHC0 "C176630" @default.
- NCIT_C176630 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176630 NCIT_P108 "Immunodeficiency 11B with Atopic Dermatitis" @default.
- NCIT_C176630 NCIT_P208 "CL786201" @default.
- NCIT_C176630 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176630 NCIT_R176 NCIT_C20462 @default.
- NCIT_C176630 NCIT_R176 NCIT_C60668 @default.
- NCIT_C176630 normalizedInformationContent "100" @default.
- NCIT_C176630 referenceCount "1" @default.
- NCIT_C176630 hasExactSynonym "Atopic Dermatitis, Elevated IgE, and Eosinophilia" @default.
- NCIT_C176630 hasExactSynonym "CARD11/CID" @default.
- NCIT_C176630 hasExactSynonym "IMD11B" @default.
- NCIT_C176630 hasExactSynonym "Immunodeficiency 11B with Atopic Dermatitis" @default.
- NCIT_C176630 type Class @default.
- NCIT_C176630 isDefinedBy ncit.owl @default.
- NCIT_C176630 label "Immunodeficiency 11B with Atopic Dermatitis" @default.
- NCIT_C176630 subClassOf B619d7833e2329bbd268fac9ec0816599 @default.
- NCIT_C176630 subClassOf B8ae0810676f0e972f5497eaa134bae3f @default.
- NCIT_C176630 subClassOf NCIT_C176630 @default.
- NCIT_C176630 subClassOf NCIT_C27351 @default.
- NCIT_C176630 subClassOf NCIT_C27551 @default.
- NCIT_C176630 subClassOf NCIT_C28193 @default.
- NCIT_C176630 subClassOf NCIT_C2991 @default.
- NCIT_C176630 subClassOf NCIT_C3131 @default.
- NCIT_C176630 subClassOf NCIT_C3507 @default.
- NCIT_C176630 subClassOf NCIT_C7057 @default.