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Q30371477-4814A792-F9E8-425B-913C-E7662232314D
Q30371477-4814A792-F9E8-425B-913C-E7662232314D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30371477-4814A792-F9E8-425B-913C-E7662232314D
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes.
P698
Q30371477-4814A792-F9E8-425B-913C-E7662232314D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30371477-4814A792-F9E8-425B-913C-E7662232314D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
f736ed701b37ea7a357869800bc9cd3c22be8621
P698
25655089
http://www.w3.org/2001/XMLSchema#string