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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/43BB540F93518A7673E4E1665F751D728440CF0E0E5F0800FA951AE22B79DA4DDC49BC3E4F532CB61391A2F9DF6E5B58>
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http://purl.uniprot.org/SHA-384/43BB540F93518A7673E4E1665F751D728440CF0E0E5F0800FA951AE22B79DA4DDC49BC3E4F532CB61391A2F9DF6E5B58
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/43BB540F93518A7673E4E1665F751D728440CF0E0E5F0800FA951AE22B79DA4DDC49BC3E4F532CB61391A2F9DF6E5B58
http://www.w3.org/2000/01/rdf-schema#comment
"Genetic testing identified the mutation in the EMD gene confirming X-linked recessive (XR) EDMD. The patient's asymptomatic mother was confirmed as a carrier."
xsd:string
http://purl.uniprot.org/uniprot/#_B266420E277652B5B3E655DC84C9167FB60C41DB34562F9A33F64E89F7B2E83DAE144A91CDA4CC8C22E3582835093054
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/43BB540F93518A7673E4E1665F751D728440CF0E0E5F0800FA951AE22B79DA4DDC49BC3E4F532CB61391A2F9DF6E5B58
http://purl.uniprot.org/uniprot/Q5HY57
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/43BB540F93518A7673E4E1665F751D728440CF0E0E5F0800FA951AE22B79DA4DDC49BC3E4F532CB61391A2F9DF6E5B58
http://purl.uniprot.org/uniprot/#_Q5HY57-mappedCitation-22480903
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/43BB540F93518A7673E4E1665F751D728440CF0E0E5F0800FA951AE22B79DA4DDC49BC3E4F532CB61391A2F9DF6E5B58