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Q36695120-20C3DBA1-18E9-4672-B0EB-F31CACAD6241
Q36695120-20C3DBA1-18E9-4672-B0EB-F31CACAD6241
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-20C3DBA1-18E9-4672-B0EB-F31CACAD6241
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.
P2860
Q36695120-20C3DBA1-18E9-4672-B0EB-F31CACAD6241
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-20C3DBA1-18E9-4672-B0EB-F31CACAD6241
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Statement
wasDerivedFrom
3a47e51cd72fa8e7ffa013b1e8583aa97a973008
P2860
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.