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- NCIT_C27070 IAO_0000115 "A rare severe combined immunodeficiency disorder characterized by congenital agranulocytosis, lymphoid tissue and thymic tissue hypoplasia, and lymphopenia. Both cellular and humoral immunities are absent." @default.
- NCIT_C27070 NCIT_NHC0 "C27070" @default.
- NCIT_C27070 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C27070 NCIT_P108 "Reticular Dysgenesis" @default.
- NCIT_C27070 NCIT_P207 "C0272167" @default.
- NCIT_C27070 NCIT_P366 "Reticular_Dysgenesis" @default.
- NCIT_C27070 normalizedInformationContent "100" @default.
- NCIT_C27070 referenceCount "1" @default.
- NCIT_C27070 hasExactSynonym "Reticular Dysgenesis" @default.
- NCIT_C27070 type Class @default.
- NCIT_C27070 isDefinedBy ncit.owl @default.
- NCIT_C27070 label "Reticular Dysgenesis" @default.
- NCIT_C27070 subClassOf NCIT_C27070 @default.
- NCIT_C27070 subClassOf NCIT_C27351 @default.
- NCIT_C27070 subClassOf NCIT_C27551 @default.
- NCIT_C27070 subClassOf NCIT_C27871 @default.
- NCIT_C27070 subClassOf NCIT_C28193 @default.
- NCIT_C27070 subClassOf NCIT_C2991 @default.
- NCIT_C27070 subClassOf NCIT_C3101 @default.
- NCIT_C27070 subClassOf NCIT_C3131 @default.
- NCIT_C27070 subClassOf NCIT_C3507 @default.
- NCIT_C27070 subClassOf NCIT_C7057 @default.