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Q44304571-173AFB14-C787-46D2-BC1F-E929577A15A9
Q44304571-173AFB14-C787-46D2-BC1F-E929577A15A9
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Statement
http://www.wikidata.org/entity/statement/Q44304571-173AFB14-C787-46D2-BC1F-E929577A15A9
A complex genomic abnormality found in a patient with antithrombin deficiency and autoimmune disease-like symptoms.
P2860
Q44304571-173AFB14-C787-46D2-BC1F-E929577A15A9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44304571-173AFB14-C787-46D2-BC1F-E929577A15A9
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Statement
wasDerivedFrom
1e9f5b1f2948ea379f4f093b2dee0364e5966d00
P2860
The phenotypic and genetic assessment of antithrombin deficiency.