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- NCIT_C185533 IAO_0000115 "A genetic finding indicating that both copies of chromosome 16 each have a copy of the hemoglobin beta gene (HBB) with loss of function or gene deletion mutations (B0). This genotype is associated with beta thalassemia major." @default.
- NCIT_C185533 NCIT_A13 NCIT_C84951 @default.
- NCIT_C185533 NCIT_NHC0 "C185533" @default.
- NCIT_C185533 NCIT_P106 "Laboratory or Test Result" @default.
- NCIT_C185533 NCIT_P108 "Hemoglobin Beta Homozygous Null Genotype" @default.
- NCIT_C185533 NCIT_P208 "CL1773720" @default.
- NCIT_C185533 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C185533 referenceCount "2" @default.
- NCIT_C185533 hasExactSynonym "(B0/B0)" @default.
- NCIT_C185533 hasExactSynonym "B0/B0" @default.
- NCIT_C185533 hasExactSynonym "HBB Homozygous Null Genotype" @default.
- NCIT_C185533 hasExactSynonym "HBB Null Genotype" @default.
- NCIT_C185533 hasExactSynonym "Hemoglobin Beta Homozygous Null Genotype" @default.
- NCIT_C185533 hasExactSynonym "beta-globin genotype (B0/B0)" @default.
- NCIT_C185533 type Class @default.
- NCIT_C185533 isDefinedBy ncit.owl @default.
- NCIT_C185533 label "Hemoglobin Beta Homozygous Null Genotype" @default.
- NCIT_C185533 subClassOf NCIT_C103223 @default.
- NCIT_C185533 subClassOf NCIT_C185500 @default.
- NCIT_C185533 subClassOf NCIT_C185523 @default.
- NCIT_C185533 subClassOf NCIT_C185533 @default.
- NCIT_C185533 subClassOf NCIT_C3367 @default.
- NCIT_C185533 subClassOf NCIT_C36292 @default.
- NCIT_C185533 subClassOf NCIT_C7057 @default.
- NCIT_C185533 subClassOf NCIT_C77140 @default.