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Q24618688-1F4C0132-E817-4EE4-B36E-042F190A4696
Q24618688-1F4C0132-E817-4EE4-B36E-042F190A4696
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24618688-1F4C0132-E817-4EE4-B36E-042F190A4696
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association
P2860
Q24618688-1F4C0132-E817-4EE4-B36E-042F190A4696
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24618688-1F4C0132-E817-4EE4-B36E-042F190A4696
rank
NormalRank
type
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Statement
wasDerivedFrom
63beb7e5641362eb32af1249665917039131c54f
P2860
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane