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- NCIT_C91500 NCIT_NHC0 "C91500" @default.
- NCIT_C91500 NCIT_P106 "Functional Concept" @default.
- NCIT_C91500 NCIT_P108 "Primary Immunodeficiency Pathway" @default.
- NCIT_C91500 NCIT_P207 "C2984310" @default.
- NCIT_C91500 NCIT_P215 "hsa05340" @default.
- NCIT_C91500 NCIT_P325 "Primary immunodeficiencies (PIs) are a heterogeneous group of disorders, which affect cellular and humoral immunity or non-specific host defense mechanisms mediated by complement proteins, and cells such as phagocytes and natural killer (NK) cells. These disorders of the immune system cause increased susceptibility to infection, autoimmune disease, and malignancy. Most of PIs are due to genetic defects that affect cell maturation or function at different levels during hematopoiesis. Disruption of the cellular immunity is observed in patients with defects in T cells or both T and B cells. These cellular immunodeficiencies comprise 20% of all PIs. Disorders of humoral immunity affect B-cell differentiation and antibody production. They account for 70% of all PIs." @default.
- NCIT_C91500 normalizedInformationContent "72.176867223268616" @default.
- NCIT_C91500 referenceCount "67" @default.
- NCIT_C91500 hasExactSynonym "Primary Immunodeficiency Pathway" @default.
- NCIT_C91500 hasExactSynonym "Primary immunodeficiency" @default.
- NCIT_C91500 type Class @default.
- NCIT_C91500 isDefinedBy ncit.owl @default.
- NCIT_C91500 label "Primary Immunodeficiency Pathway" @default.
- NCIT_C91500 subClassOf NCIT_C20633 @default.
- NCIT_C91500 subClassOf NCIT_C39701 @default.
- NCIT_C91500 subClassOf NCIT_C91500 @default.