Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
hemoglobin
|
| gptkbp:abbreviation |
gptkb:HbC
|
| gptkbp:affects |
oxygen transport
|
| gptkbp:associatedWith |
gptkb:hemoglobin_C_disease
mild hemolytic anemia |
| gptkbp:discoveredBy |
gptkb:James_V._Neel
|
| gptkbp:discoveredIn |
1950
|
| gptkbp:electrophoresis_mobility |
slower than hemoglobin A
|
| gptkbp:encodedBy |
gptkb:HBB_gene
|
| gptkbp:form |
gptkb:hemoglobin_SC_disease_(with_hemoglobin_S)
|
| gptkbp:foundIn |
humans
|
| gptkbp:has_mutation |
gptkb:beta-globin_gene
|
| https://www.w3.org/2000/01/rdf-schema#label |
hemoglobin C
|
| gptkbp:inherited_as |
autosomal recessive trait
|
| gptkbp:mutationAssociatedWith |
glutamic acid to lysine substitution at position 6
|
| gptkbp:prevalence |
gptkb:African-American
gptkb:West_Africa |
| gptkbp:bfsParent |
gptkb:hemoglobin
|
| gptkbp:bfsLayer |
5
|