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- NCIT_C176823 IAO_0000115 "A genetic disorder caused by molecular defects in the genes encoding for four regulatory factors controlling transcription of MHC class II genes. The phenotype is similar to SCID, and susceptibility to infection by viral, bacterial, fungal and protozoal agents is characteristic of the disease." @default.
- NCIT_C176823 NCIT_NHC0 "C176823" @default.
- NCIT_C176823 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176823 NCIT_P108 "MHC Class II Deficiency" @default.
- NCIT_C176823 NCIT_P208 "CL1642592" @default.
- NCIT_C176823 NCIT_R116 NCIT_C150672 @default.
- NCIT_C176823 NCIT_R116 NCIT_C150673 @default.
- NCIT_C176823 NCIT_R116 NCIT_C26323 @default.
- NCIT_C176823 NCIT_R116 NCIT_C27351 @default.
- NCIT_C176823 NCIT_R116 NCIT_C27551 @default.
- NCIT_C176823 NCIT_R116 NCIT_C2991 @default.
- NCIT_C176823 NCIT_R116 NCIT_C35686 @default.
- NCIT_C176823 NCIT_R116 NCIT_C35814 @default.
- NCIT_C176823 NCIT_R116 NCIT_C7057 @default.
- NCIT_C176823 NCIT_R116 NCIT_C9308 @default.
- NCIT_C176823 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C176823 referenceCount "2" @default.
- NCIT_C176823 hasExactSynonym "MHC Class II Deficiency" @default.
- NCIT_C176823 hasExactSynonym "MHC class II deficiency" @default.
- NCIT_C176823 type Class @default.
- NCIT_C176823 isDefinedBy ncit.owl @default.
- NCIT_C176823 label "MHC Class II Deficiency" @default.
- NCIT_C176823 subClassOf NCIT_C176823 @default.
- NCIT_C176823 subClassOf NCIT_C27351 @default.
- NCIT_C176823 subClassOf NCIT_C27551 @default.
- NCIT_C176823 subClassOf NCIT_C27871 @default.
- NCIT_C176823 subClassOf NCIT_C28193 @default.
- NCIT_C176823 subClassOf NCIT_C2991 @default.
- NCIT_C176823 subClassOf NCIT_C3101 @default.
- NCIT_C176823 subClassOf NCIT_C3131 @default.
- NCIT_C176823 subClassOf NCIT_C3472 @default.
- NCIT_C176823 subClassOf NCIT_C3507 @default.
- NCIT_C176823 subClassOf NCIT_C7057 @default.