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DESCRIBE <http://purl.uniprot.org/SHA-384/7F75B50C6B19F7311D090DEFB7544DFA0E5EA45DBE03B5289AC2833F4B65933F169D4BA3F1C68E76074DFD5DB3805948>
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http://purl.uniprot.org/SHA-384/7F75B50C6B19F7311D090DEFB7544DFA0E5EA45DBE03B5289AC2833F4B65933F169D4BA3F1C68E76074DFD5DB3805948
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7F75B50C6B19F7311D090DEFB7544DFA0E5EA45DBE03B5289AC2833F4B65933F169D4BA3F1C68E76074DFD5DB3805948
http://www.w3.org/2000/01/rdf-schema#comment
"Smith-Magenis syndrome is caused by a de novo deletion on chromosome 17."
xsd:string
http://purl.uniprot.org/uniprot/#_67D1E3C33A5F6C456A2EEB257CB9B96EDCE9D1F9A987786DEB01AF8890B85ECA3C3113FF910D540944FD2A3AE6AE73D1
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7F75B50C6B19F7311D090DEFB7544DFA0E5EA45DBE03B5289AC2833F4B65933F169D4BA3F1C68E76074DFD5DB3805948
http://purl.uniprot.org/uniprot/Q96C03
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7F75B50C6B19F7311D090DEFB7544DFA0E5EA45DBE03B5289AC2833F4B65933F169D4BA3F1C68E76074DFD5DB3805948
http://purl.uniprot.org/uniprot/#_Q96C03-mappedCitation-15517828
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7F75B50C6B19F7311D090DEFB7544DFA0E5EA45DBE03B5289AC2833F4B65933F169D4BA3F1C68E76074DFD5DB3805948