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- NCIT_C176825 IAO_0000115 "A genetic condition caused by mutation(s) in the IRF8 gene encoding interferon regulatory factor 8. Autosomal dominant (Immunodeficiency 32A) and autosomal recessive (Immunodeficiency 32B) genetic alterations result in different phenotypes, both of which have impairment of function in dendritic cells." @default.
- NCIT_C176825 NCIT_NHC0 "C176825" @default.
- NCIT_C176825 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176825 NCIT_P108 "Interferon Regulatory Factor 8 Deficiency" @default.
- NCIT_C176825 NCIT_P208 "CL1642591" @default.
- NCIT_C176825 NCIT_R176 NCIT_C104554 @default.
- NCIT_C176825 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176825 NCIT_R176 NCIT_C20673 @default.
- NCIT_C176825 NCIT_R176 NCIT_C20710 @default.
- NCIT_C176825 NCIT_R176 NCIT_C54362 @default.
- NCIT_C176825 normalizedInformationContent "100" @default.
- NCIT_C176825 referenceCount "1" @default.
- NCIT_C176825 hasExactSynonym "IRF8 Deficiency" @default.
- NCIT_C176825 hasExactSynonym "IRF8, Dendritic cell immunodeficiency" @default.
- NCIT_C176825 hasExactSynonym "Interferon Regulatory Factor 8 Deficiency" @default.
- NCIT_C176825 type Class @default.
- NCIT_C176825 isDefinedBy ncit.owl @default.
- NCIT_C176825 label "Interferon Regulatory Factor 8 Deficiency" @default.
- NCIT_C176825 subClassOf B0f4a7ea9c54e35679c49e01c9f989b82 @default.
- NCIT_C176825 subClassOf B117cfb4845d6b06a6ed88208c04c5f35 @default.
- NCIT_C176825 subClassOf NCIT_C176825 @default.
- NCIT_C176825 subClassOf NCIT_C27351 @default.
- NCIT_C176825 subClassOf NCIT_C27551 @default.
- NCIT_C176825 subClassOf NCIT_C28193 @default.
- NCIT_C176825 subClassOf NCIT_C2991 @default.
- NCIT_C176825 subClassOf NCIT_C3131 @default.
- NCIT_C176825 subClassOf NCIT_C3507 @default.
- NCIT_C176825 subClassOf NCIT_C7057 @default.