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DESCRIBE <http://purl.uniprot.org/SHA-384/2ECA8DE284D3AE327C814E35F348DE403EFED8032845F0ABD43ACDF6D979DF4A8119F4912FA790B81880F18EF2583271>
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http://purl.uniprot.org/SHA-384/2ECA8DE284D3AE327C814E35F348DE403EFED8032845F0ABD43ACDF6D979DF4A8119F4912FA790B81880F18EF2583271
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2ECA8DE284D3AE327C814E35F348DE403EFED8032845F0ABD43ACDF6D979DF4A8119F4912FA790B81880F18EF2583271
http://www.w3.org/2000/01/rdf-schema#comment
"IQSEC2 mutation is associated with syndromic intellectual disability."
xsd:string
http://purl.uniprot.org/uniprot/#_4F34428D2BB0E621DF6CD24692CE0B822D96F4FE9455FE1316848F1F1BD86D37FA088BF7F1DBEDEE08660AE6CFB4C756
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2ECA8DE284D3AE327C814E35F348DE403EFED8032845F0ABD43ACDF6D979DF4A8119F4912FA790B81880F18EF2583271
http://purl.uniprot.org/uniprot/C7SDG0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2ECA8DE284D3AE327C814E35F348DE403EFED8032845F0ABD43ACDF6D979DF4A8119F4912FA790B81880F18EF2583271
http://purl.uniprot.org/uniprot/#_C7SDG0-mappedCitation-28815955
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2ECA8DE284D3AE327C814E35F348DE403EFED8032845F0ABD43ACDF6D979DF4A8119F4912FA790B81880F18EF2583271