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- NCIT_C176820 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the WIPF1 gene, encoding WAS/WASL-interacting protein family member 1. It is characterized by recurrent infections, eczema, thrombocytopenia, and T-cell and NK-cell dysfunction." @default.
- NCIT_C176820 NCIT_NHC0 "C176820" @default.
- NCIT_C176820 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176820 NCIT_P108 "Wiskott-Aldrich Syndrome 2" @default.
- NCIT_C176820 NCIT_P207 "C4016786" @default.
- NCIT_C176820 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176820 NCIT_R176 NCIT_C176613 @default.
- NCIT_C176820 NCIT_R176 NCIT_C20744 @default.
- NCIT_C176820 NCIT_R176 NCIT_C20745 @default.
- NCIT_C176820 normalizedInformationContent "100" @default.
- NCIT_C176820 referenceCount "1" @default.
- NCIT_C176820 hasExactSynonym "WAS2" @default.
- NCIT_C176820 hasExactSynonym "WIP Deficiency" @default.
- NCIT_C176820 hasExactSynonym "Wiskott-Aldrich Syndrome 2" @default.
- NCIT_C176820 hasExactSynonym "Wiskott-Aldrich Syndrome Interacting Protein Deficiency" @default.
- NCIT_C176820 type Class @default.
- NCIT_C176820 isDefinedBy ncit.owl @default.
- NCIT_C176820 label "Wiskott-Aldrich Syndrome 2" @default.
- NCIT_C176820 subClassOf B2449bdbfc5c892ac199ee12d39ad607e @default.
- NCIT_C176820 subClassOf Bac9e59315610fa93848c7e3437e21430 @default.
- NCIT_C176820 subClassOf NCIT_C176820 @default.
- NCIT_C176820 subClassOf NCIT_C27351 @default.
- NCIT_C176820 subClassOf NCIT_C27551 @default.
- NCIT_C176820 subClassOf NCIT_C27871 @default.
- NCIT_C176820 subClassOf NCIT_C28193 @default.
- NCIT_C176820 subClassOf NCIT_C2991 @default.
- NCIT_C176820 subClassOf NCIT_C3101 @default.
- NCIT_C176820 subClassOf NCIT_C3131 @default.
- NCIT_C176820 subClassOf NCIT_C3507 @default.
- NCIT_C176820 subClassOf NCIT_C7057 @default.