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- NCIT_C176819 IAO_0000115 "An autosomal dominant immunodeficiency syndrome caused by mutation(s) in the CXCR4 gene, encoding C-X-C chemokine receptor type 4. It is characterized by neutropenia, hypogammaglobulinemia, extensive human papillomavirus (HPV) infection, and myelokathexis." @default.
- NCIT_C176819 NCIT_NHC0 "C176819" @default.
- NCIT_C176819 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176819 NCIT_P108 "Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome" @default.
- NCIT_C176819 NCIT_P207 "C0472817" @default.
- NCIT_C176819 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176819 NCIT_R176 NCIT_C20103 @default.
- NCIT_C176819 NCIT_R176 NCIT_C20912 @default.
- NCIT_C176819 NCIT_R176 NCIT_C20923 @default.
- NCIT_C176819 NCIT_R176 NCIT_C21295 @default.
- NCIT_C176819 NCIT_R176 NCIT_C24327 @default.
- NCIT_C176819 NCIT_R176 NCIT_C25775 @default.
- NCIT_C176819 normalizedInformationContent "100" @default.
- NCIT_C176819 referenceCount "1" @default.
- NCIT_C176819 hasExactSynonym "WHIM Syndrome" @default.
- NCIT_C176819 hasExactSynonym "WHIM" @default.
- NCIT_C176819 hasExactSynonym "WHIMS" @default.
- NCIT_C176819 hasExactSynonym "Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome" @default.
- NCIT_C176819 type Class @default.
- NCIT_C176819 isDefinedBy ncit.owl @default.
- NCIT_C176819 label "Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome" @default.
- NCIT_C176819 subClassOf B4f8523d621488001c4d452ddb67e537e @default.
- NCIT_C176819 subClassOf B86b42414547ad34ae56538362b08ca21 @default.
- NCIT_C176819 subClassOf NCIT_C176819 @default.
- NCIT_C176819 subClassOf NCIT_C28193 @default.
- NCIT_C176819 subClassOf NCIT_C2991 @default.
- NCIT_C176819 subClassOf NCIT_C7057 @default.