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Q38047367-1A902298-0ABB-42DC-962C-1E6204421F7D
Q38047367-1A902298-0ABB-42DC-962C-1E6204421F7D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38047367-1A902298-0ABB-42DC-962C-1E6204421F7D
Congenital defects of platelet function.
P2860
Q38047367-1A902298-0ABB-42DC-962C-1E6204421F7D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38047367-1A902298-0ABB-42DC-962C-1E6204421F7D
rank
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type
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Statement
wasDerivedFrom
42c3391425911531373304c9248cdca420c69cc1
P2860
Arg60 to Leu mutation of the human thromboxane A2 receptor in a dominantly inherited bleeding disorder