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DESCRIBE <http://purl.uniprot.org/SHA-384/4972B497DEE03284C34EDEDC16574753A4A00DFFE8AC6EE28B751062219C5A10031E5F6C29922C9735134C33CFB74DD2>
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http://purl.uniprot.org/SHA-384/4972B497DEE03284C34EDEDC16574753A4A00DFFE8AC6EE28B751062219C5A10031E5F6C29922C9735134C33CFB74DD2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4972B497DEE03284C34EDEDC16574753A4A00DFFE8AC6EE28B751062219C5A10031E5F6C29922C9735134C33CFB74DD2
http://www.w3.org/2000/01/rdf-schema#comment
"We report a 2p13.2 microdeletion in 2 subjects encompasing 2 genes EXOC6B and CYP26B12 with clinical effects on cognitive function and craniofacial and skeletal development."
xsd:string
http://purl.uniprot.org/uniprot/#_A681A79BDB7AB210A8E7932342CC1F1DC081ED3067A85193B1F93496223C464189BD4ED0DD16AA5358C6E53F6852EB7E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4972B497DEE03284C34EDEDC16574753A4A00DFFE8AC6EE28B751062219C5A10031E5F6C29922C9735134C33CFB74DD2
http://purl.uniprot.org/uniprot/Q9Y2D4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4972B497DEE03284C34EDEDC16574753A4A00DFFE8AC6EE28B751062219C5A10031E5F6C29922C9735134C33CFB74DD2
http://purl.uniprot.org/uniprot/#_Q9Y2D4-mappedCitation-23837398
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4972B497DEE03284C34EDEDC16574753A4A00DFFE8AC6EE28B751062219C5A10031E5F6C29922C9735134C33CFB74DD2