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- NCIT_C176805 IAO_0000115 "A genetic condition caused by mutation(s) in the IFNGR2 gene, encoding interferon gamma receptor 2, resulting in impairment of interferon-gamma mediated immunity. Clinically, it is characterized by predisposition to illness caused by moderately virulent mycobacterial species." @default.
- NCIT_C176805 NCIT_NHC0 "C176805" @default.
- NCIT_C176805 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176805 NCIT_P108 "Interferon Gamma Receptor 2 Deficiency" @default.
- NCIT_C176805 NCIT_P207 "C4013947" @default.
- NCIT_C176805 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176805 NCIT_R176 NCIT_C20103 @default.
- NCIT_C176805 NCIT_R176 NCIT_C20912 @default.
- NCIT_C176805 NCIT_R176 NCIT_C21295 @default.
- NCIT_C176805 NCIT_R176 NCIT_C37287 @default.
- NCIT_C176805 normalizedInformationContent "100" @default.
- NCIT_C176805 referenceCount "1" @default.
- NCIT_C176805 hasExactSynonym "IFNGR 2 Deficiency" @default.
- NCIT_C176805 hasExactSynonym "IFNGR2 Deficiency" @default.
- NCIT_C176805 hasExactSynonym "Interferon Gamma Receptor 2 Deficiency" @default.
- NCIT_C176805 type Class @default.
- NCIT_C176805 isDefinedBy ncit.owl @default.
- NCIT_C176805 label "Interferon Gamma Receptor 2 Deficiency" @default.
- NCIT_C176805 subClassOf B53938c047eccf55793c825e891f3cdde @default.
- NCIT_C176805 subClassOf Bfbd6d9aa316567bddf2e31f1afac7aff @default.
- NCIT_C176805 subClassOf NCIT_C176805 @default.
- NCIT_C176805 subClassOf NCIT_C27351 @default.
- NCIT_C176805 subClassOf NCIT_C27551 @default.
- NCIT_C176805 subClassOf NCIT_C28193 @default.
- NCIT_C176805 subClassOf NCIT_C2991 @default.
- NCIT_C176805 subClassOf NCIT_C3131 @default.
- NCIT_C176805 subClassOf NCIT_C3507 @default.
- NCIT_C176805 subClassOf NCIT_C7057 @default.