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- NCIT_C185525 IAO_0000115 "A genetic finding indicating that both copies of chromosome 16 each have a copy of the hemoglobin beta gene (HBB) with mutations that lead to hemoglobin subunit beta insufficiency (B+). This genotype is associated with beta thalassemia intermedia." @default.
- NCIT_C185525 NCIT_A13 NCIT_C84951 @default.
- NCIT_C185525 NCIT_NHC0 "C185525" @default.
- NCIT_C185525 NCIT_P106 "Laboratory or Test Result" @default.
- NCIT_C185525 NCIT_P108 "Hemoglobin Beta Homozygous Insufficient Genotype" @default.
- NCIT_C185525 NCIT_P208 "CL1773702" @default.
- NCIT_C185525 normalizedInformationContent "100" @default.
- NCIT_C185525 referenceCount "1" @default.
- NCIT_C185525 hasExactSynonym "(B+/B+)" @default.
- NCIT_C185525 hasExactSynonym "B+/B+" @default.
- NCIT_C185525 hasExactSynonym "HBB Homozygous Insufficient Genotype" @default.
- NCIT_C185525 hasExactSynonym "HBB Insufficient Genotype" @default.
- NCIT_C185525 hasExactSynonym "Hemoglobin Beta Homozygous Insufficient Genotype" @default.
- NCIT_C185525 hasExactSynonym "beta-globin genotype (B+/B+)" @default.
- NCIT_C185525 type Class @default.
- NCIT_C185525 isDefinedBy ncit.owl @default.
- NCIT_C185525 label "Hemoglobin Beta Homozygous Insufficient Genotype" @default.
- NCIT_C185525 subClassOf NCIT_C103223 @default.
- NCIT_C185525 subClassOf NCIT_C185500 @default.
- NCIT_C185525 subClassOf NCIT_C185523 @default.
- NCIT_C185525 subClassOf NCIT_C185525 @default.
- NCIT_C185525 subClassOf NCIT_C3367 @default.
- NCIT_C185525 subClassOf NCIT_C36292 @default.
- NCIT_C185525 subClassOf NCIT_C7057 @default.
- NCIT_C185525 subClassOf NCIT_C77140 @default.