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DESCRIBE <http://purl.uniprot.org/SHA-384/9EC3EB608D8343CB402209DE4B00C4CEC8B511A5B6C0C7A302F211FD2CBD83D60DC29040D18DBE8B270EB31012A35A45>
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http://purl.uniprot.org/SHA-384/9EC3EB608D8343CB402209DE4B00C4CEC8B511A5B6C0C7A302F211FD2CBD83D60DC29040D18DBE8B270EB31012A35A45
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9EC3EB608D8343CB402209DE4B00C4CEC8B511A5B6C0C7A302F211FD2CBD83D60DC29040D18DBE8B270EB31012A35A45
http://www.w3.org/2000/01/rdf-schema#comment
"Description of a novel ARFGEF2 mutation in five related patients presenting with West syndrome microcephaly periventricular heterotopia and thin corpus callosum."
xsd:string
http://purl.uniprot.org/uniprot/#_8E0BCF26F67FADDA01628A8BDA3235D6B5C33A552F84706BC58B519DEF9B79CC13A37E929EB6BB6D78D261AC31B8D5BC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9EC3EB608D8343CB402209DE4B00C4CEC8B511A5B6C0C7A302F211FD2CBD83D60DC29040D18DBE8B270EB31012A35A45
http://purl.uniprot.org/uniprot/Q86TH5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9EC3EB608D8343CB402209DE4B00C4CEC8B511A5B6C0C7A302F211FD2CBD83D60DC29040D18DBE8B270EB31012A35A45
http://purl.uniprot.org/uniprot/#_Q86TH5-mappedCitation-23812912
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9EC3EB608D8343CB402209DE4B00C4CEC8B511A5B6C0C7A302F211FD2CBD83D60DC29040D18DBE8B270EB31012A35A45