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Q36695120-0C044DF8-59C5-4E25-98B9-49AC98C66B3B
Q36695120-0C044DF8-59C5-4E25-98B9-49AC98C66B3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-0C044DF8-59C5-4E25-98B9-49AC98C66B3B
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.
P2860
Q36695120-0C044DF8-59C5-4E25-98B9-49AC98C66B3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-0C044DF8-59C5-4E25-98B9-49AC98C66B3B
rank
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type
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Statement
wasDerivedFrom
3a47e51cd72fa8e7ffa013b1e8583aa97a973008
P2860
Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome