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http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/volume"94"xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Field M."xsd:string
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http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Archer H."xsd:string
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http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Hackett A."xsd:string
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http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Parker M.J."xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Spasic-Boskovic O."xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Firth H.V."xsd:string
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http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Carss K."xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Canham N."xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/title"De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability."xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Grozeva D."xsd:string
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Wilson M."xsd:string
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http://purl.uniprot.org/citations/24680889http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/uniprot/#_Q9C0A6-citation-24680889http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24680889
http://purl.uniprot.org/citations/24680889http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24680889
http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/name"Am. J. Hum. Genet."xsd:string
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http://purl.uniprot.org/citations/24680889http://purl.uniprot.org/core/author"Floyd J.A."xsd:string