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- NCIT_C185582 IAO_0000115 "A genetic finding indicating that one copy of chromosome 16 has a functional copy (B) of the hemoglobin beta gene (HBB) and the other copy has HBB loss of function or gene deletion mutations (B0). This genotype is associated with beta thalassemia minor." @default.
- NCIT_C185582 NCIT_A13 NCIT_C84951 @default.
- NCIT_C185582 NCIT_NHC0 "C185582" @default.
- NCIT_C185582 NCIT_P106 "Laboratory or Test Result" @default.
- NCIT_C185582 NCIT_P108 "Hemoglobin Beta Heterozygous Null Genotype" @default.
- NCIT_C185582 NCIT_P208 "CL1773933" @default.
- NCIT_C185582 normalizedInformationContent "100" @default.
- NCIT_C185582 referenceCount "1" @default.
- NCIT_C185582 hasExactSynonym "(B/B0)" @default.
- NCIT_C185582 hasExactSynonym "(B0/B)" @default.
- NCIT_C185582 hasExactSynonym "B/B0" @default.
- NCIT_C185582 hasExactSynonym "B0/B" @default.
- NCIT_C185582 hasExactSynonym "HBB Heterozygous Null Genotype" @default.
- NCIT_C185582 hasExactSynonym "Hemoglobin Beta Heterozygous Null Genotype" @default.
- NCIT_C185582 hasExactSynonym "beta-globin genotype (B/B0)" @default.
- NCIT_C185582 type Class @default.
- NCIT_C185582 isDefinedBy ncit.owl @default.
- NCIT_C185582 label "Hemoglobin Beta Heterozygous Null Genotype" @default.
- NCIT_C185582 subClassOf NCIT_C103223 @default.
- NCIT_C185582 subClassOf NCIT_C185500 @default.
- NCIT_C185582 subClassOf NCIT_C185523 @default.
- NCIT_C185582 subClassOf NCIT_C185582 @default.
- NCIT_C185582 subClassOf NCIT_C3367 @default.
- NCIT_C185582 subClassOf NCIT_C36292 @default.
- NCIT_C185582 subClassOf NCIT_C7057 @default.
- NCIT_C185582 subClassOf NCIT_C77140 @default.