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DESCRIBE <http://purl.uniprot.org/SHA-384/1629988603C78C190CD1B922A704AB9FFEA020CB91B14683ABEFF1A7AAA1B59F43F0B63864FF0C5C35FBCF0A920A9972>
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http://purl.uniprot.org/SHA-384/1629988603C78C190CD1B922A704AB9FFEA020CB91B14683ABEFF1A7AAA1B59F43F0B63864FF0C5C35FBCF0A920A9972
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1629988603C78C190CD1B922A704AB9FFEA020CB91B14683ABEFF1A7AAA1B59F43F0B63864FF0C5C35FBCF0A920A9972
http://www.w3.org/2000/01/rdf-schema#comment
"Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutations"
xsd:string
http://purl.uniprot.org/uniprot/#_CC20B1B686B32881B7FDB1571F604786B344C6849AC9E38B80342DC40A52D493311D56839043C9B5FA7B795407ABEA06
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1629988603C78C190CD1B922A704AB9FFEA020CB91B14683ABEFF1A7AAA1B59F43F0B63864FF0C5C35FBCF0A920A9972
http://purl.uniprot.org/uniprot/E5KLJ9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1629988603C78C190CD1B922A704AB9FFEA020CB91B14683ABEFF1A7AAA1B59F43F0B63864FF0C5C35FBCF0A920A9972
http://purl.uniprot.org/uniprot/#_E5KLJ9-mappedCitation-21636302
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1629988603C78C190CD1B922A704AB9FFEA020CB91B14683ABEFF1A7AAA1B59F43F0B63864FF0C5C35FBCF0A920A9972