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DESCRIBE <http://purl.uniprot.org/SHA-384/94AA60ADA363503D142683189BAA7E22273B971FAC61B08133B5EDC8FB1A531E32D2057DEB1CEA6AD8DEA420EC4FB32A>
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http://purl.uniprot.org/SHA-384/94AA60ADA363503D142683189BAA7E22273B971FAC61B08133B5EDC8FB1A531E32D2057DEB1CEA6AD8DEA420EC4FB32A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/94AA60ADA363503D142683189BAA7E22273B971FAC61B08133B5EDC8FB1A531E32D2057DEB1CEA6AD8DEA420EC4FB32A
http://www.w3.org/2000/01/rdf-schema#comment
"Strong candidate gene for mitochondrial disease based on recessive mutations detected in infantile patients"
xsd:string
http://purl.uniprot.org/uniprot/#_A22149DFF84B96E610B9A7BA78F884E1AE4C0E89CA681166D475B6A4EFFA98CAA9E0D80E7EED456A205550AC2261088A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/94AA60ADA363503D142683189BAA7E22273B971FAC61B08133B5EDC8FB1A531E32D2057DEB1CEA6AD8DEA420EC4FB32A
http://purl.uniprot.org/uniprot/Q9UI02
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/94AA60ADA363503D142683189BAA7E22273B971FAC61B08133B5EDC8FB1A531E32D2057DEB1CEA6AD8DEA420EC4FB32A
http://purl.uniprot.org/uniprot/#_Q9UI02-mappedCitation-22277967
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/94AA60ADA363503D142683189BAA7E22273B971FAC61B08133B5EDC8FB1A531E32D2057DEB1CEA6AD8DEA420EC4FB32A