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Q49300785-B282B5AC-766A-4886-BF68-061BC6119389
Q49300785-B282B5AC-766A-4886-BF68-061BC6119389
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49300785-B282B5AC-766A-4886-BF68-061BC6119389
FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.
P2860
Q49300785-B282B5AC-766A-4886-BF68-061BC6119389
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49300785-B282B5AC-766A-4886-BF68-061BC6119389
rank
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type
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Statement
wasDerivedFrom
d6b24710a73861d9f9a2a1a9e1ace92e6cdba332
P2860
Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.