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DESCRIBE <http://purl.uniprot.org/SHA-384/A37682D6FC80E1934EFAB7C2873B0A70B7D09D5EFE8A2B7AB1EC053F9AC7C36A5A77A83090948E63C7F2B31C890633A2>
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http://purl.uniprot.org/SHA-384/A37682D6FC80E1934EFAB7C2873B0A70B7D09D5EFE8A2B7AB1EC053F9AC7C36A5A77A83090948E63C7F2B31C890633A2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A37682D6FC80E1934EFAB7C2873B0A70B7D09D5EFE8A2B7AB1EC053F9AC7C36A5A77A83090948E63C7F2B31C890633A2
http://www.w3.org/2000/01/rdf-schema#comment
"Peters Plus syndrome is a new congenital disorder of glycosylation and involves defective Omicron-glycosylation of thrombospondin type 1 repeats.("
xsd:string
http://purl.uniprot.org/uniprot/#_6CBBD971E0B2D1A1EC96D4788D61987BF6831EDD2756ACC9DBF60D93E4A05986C6D7C1206B6DBC8593062868B7D6273B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A37682D6FC80E1934EFAB7C2873B0A70B7D09D5EFE8A2B7AB1EC053F9AC7C36A5A77A83090948E63C7F2B31C890633A2
http://purl.uniprot.org/uniprot/Q6Y288
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A37682D6FC80E1934EFAB7C2873B0A70B7D09D5EFE8A2B7AB1EC053F9AC7C36A5A77A83090948E63C7F2B31C890633A2
http://purl.uniprot.org/uniprot/#_Q6Y288-mappedCitation-18199743
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A37682D6FC80E1934EFAB7C2873B0A70B7D09D5EFE8A2B7AB1EC053F9AC7C36A5A77A83090948E63C7F2B31C890633A2