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- NCIT_C176808 IAO_0000115 "An extremely rare autosomal recessive condition caused by mutation(s) in the LCK gene, encoding tyrosine-protein kinase Lck. It is characterized by T-cell dysfunction." @default.
- NCIT_C176808 NCIT_NHC0 "C176808" @default.
- NCIT_C176808 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176808 NCIT_P108 "LCK-Associated Immunodeficiency" @default.
- NCIT_C176808 NCIT_P207 "C4016253" @default.
- NCIT_C176808 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176808 NCIT_R176 NCIT_C17162 @default.
- NCIT_C176808 NCIT_R176 NCIT_C18541 @default.
- NCIT_C176808 NCIT_R176 NCIT_C21281 @default.
- NCIT_C176808 NCIT_R176 NCIT_C25870 @default.
- NCIT_C176808 NCIT_R176 NCIT_C25871 @default.
- NCIT_C176808 NCIT_R176 NCIT_C25872 @default.
- NCIT_C176808 NCIT_R176 NCIT_C25971 @default.
- NCIT_C176808 normalizedInformationContent "100" @default.
- NCIT_C176808 referenceCount "1" @default.
- NCIT_C176808 hasExactSynonym "IMD22" @default.
- NCIT_C176808 hasExactSynonym "Immunodeficiency 22" @default.
- NCIT_C176808 hasExactSynonym "LCK Deficiency (T Lymphocyte-specific protein TK)" @default.
- NCIT_C176808 hasExactSynonym "LCK Deficiency" @default.
- NCIT_C176808 hasExactSynonym "LCK-Associated Immunodeficiency" @default.
- NCIT_C176808 type Class @default.
- NCIT_C176808 isDefinedBy ncit.owl @default.
- NCIT_C176808 label "LCK-Associated Immunodeficiency" @default.
- NCIT_C176808 subClassOf B2b7c13ba6652dba6e3cdeceaf45d44f6 @default.
- NCIT_C176808 subClassOf Bd2a110d9e5668435809c4d33410741c7 @default.
- NCIT_C176808 subClassOf NCIT_C176808 @default.
- NCIT_C176808 subClassOf NCIT_C27351 @default.
- NCIT_C176808 subClassOf NCIT_C27551 @default.
- NCIT_C176808 subClassOf NCIT_C28193 @default.
- NCIT_C176808 subClassOf NCIT_C2991 @default.
- NCIT_C176808 subClassOf NCIT_C3131 @default.
- NCIT_C176808 subClassOf NCIT_C3507 @default.
- NCIT_C176808 subClassOf NCIT_C7057 @default.