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Q38656663-C402B98F-E88E-4AD7-8693-980E6EC9D4B6
Q38656663-C402B98F-E88E-4AD7-8693-980E6EC9D4B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38656663-C402B98F-E88E-4AD7-8693-980E6EC9D4B6
Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance.
P2860
Q38656663-C402B98F-E88E-4AD7-8693-980E6EC9D4B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38656663-C402B98F-E88E-4AD7-8693-980E6EC9D4B6
rank
NormalRank
type
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Statement
wasDerivedFrom
b7587aaef36a45ce22b535389fce88a2665124a6
P2860
Human genetic variation database, a reference database of genetic variations in the Japanese population.