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Q24564889-EB2E5468-08CD-4982-BE38-2DE04F50F7FE
Q24564889-EB2E5468-08CD-4982-BE38-2DE04F50F7FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24564889-EB2E5468-08CD-4982-BE38-2DE04F50F7FE
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple he
P2860
Q24564889-EB2E5468-08CD-4982-BE38-2DE04F50F7FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24564889-EB2E5468-08CD-4982-BE38-2DE04F50F7FE
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wasDerivedFrom
b1b03f9161f8b1508fa587c41f36743177107dbc
P2860
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association