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Q34184346-859EECFE-2E1C-483A-B9E3-1A6BB2AFFB3B
Q34184346-859EECFE-2E1C-483A-B9E3-1A6BB2AFFB3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34184346-859EECFE-2E1C-483A-B9E3-1A6BB2AFFB3B
A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats.
P2860
Q34184346-859EECFE-2E1C-483A-B9E3-1A6BB2AFFB3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34184346-859EECFE-2E1C-483A-B9E3-1A6BB2AFFB3B
rank
NormalRank
type
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Statement
wasDerivedFrom
7cfbf4855ec52c039b317be0bd022dad6b8bfd2b
P2860
Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.