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Q24685473-DB96CCE7-0526-4FBB-B4BC-F70947C254BA
Q24685473-DB96CCE7-0526-4FBB-B4BC-F70947C254BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24685473-DB96CCE7-0526-4FBB-B4BC-F70947C254BA
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
P2860
Q24685473-DB96CCE7-0526-4FBB-B4BC-F70947C254BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24685473-DB96CCE7-0526-4FBB-B4BC-F70947C254BA
rank
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type
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wasDerivedFrom
b1b56284fa3d1658bc4a1bae0e909c2eb60bb495
P2860
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopeni