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DESCRIBE <http://purl.uniprot.org/SHA-384/8A0D8F11569B0EF736686173466AE8C26A597B42BF0FBD7CE0134AC9D3E6006A9271117E9B52251AC9A66602D0FA71E4>
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http://purl.uniprot.org/SHA-384/8A0D8F11569B0EF736686173466AE8C26A597B42BF0FBD7CE0134AC9D3E6006A9271117E9B52251AC9A66602D0FA71E4
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/8A0D8F11569B0EF736686173466AE8C26A597B42BF0FBD7CE0134AC9D3E6006A9271117E9B52251AC9A66602D0FA71E4
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/#_8AABE9DF71297C43222F39567D66D79EF7F513990B70424A309BF3BEDDE9C0530B7E1483216184C5E3BF0274EDC284C3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/8A0D8F11569B0EF736686173466AE8C26A597B42BF0FBD7CE0134AC9D3E6006A9271117E9B52251AC9A66602D0FA71E4
http://purl.uniprot.org/uniprot/Q5JPH6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8A0D8F11569B0EF736686173466AE8C26A597B42BF0FBD7CE0134AC9D3E6006A9271117E9B52251AC9A66602D0FA71E4
http://purl.uniprot.org/uniprot/#_Q5JPH6-mappedCitation-22277967
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8A0D8F11569B0EF736686173466AE8C26A597B42BF0FBD7CE0134AC9D3E6006A9271117E9B52251AC9A66602D0FA71E4