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DESCRIBE <http://purl.uniprot.org/SHA-384/2607AD24769C794F26CA40E11F73F6AD57957BE613F06B06B445803C17797E45D2E38D24639678360B4CCDF9A8FFF6C1>
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http://purl.uniprot.org/SHA-384/2607AD24769C794F26CA40E11F73F6AD57957BE613F06B06B445803C17797E45D2E38D24639678360B4CCDF9A8FFF6C1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2607AD24769C794F26CA40E11F73F6AD57957BE613F06B06B445803C17797E45D2E38D24639678360B4CCDF9A8FFF6C1
http://www.w3.org/2000/01/rdf-schema#comment
"identification of four additional patients with mutations in ECHS1 highlights the importance of the valine degradation pathway in Leigh syndrome"
xsd:string
http://purl.uniprot.org/uniprot/#_5D0EEE6D7F77335A7DBD5E86691B28A0BB8801F6506A73C49679D83026527A6AC366A25376A19833804EA962BB676EF2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2607AD24769C794F26CA40E11F73F6AD57957BE613F06B06B445803C17797E45D2E38D24639678360B4CCDF9A8FFF6C1
http://purl.uniprot.org/uniprot/A0A384MDW7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2607AD24769C794F26CA40E11F73F6AD57957BE613F06B06B445803C17797E45D2E38D24639678360B4CCDF9A8FFF6C1
http://purl.uniprot.org/uniprot/#_A0A384MDW7-mappedCitation-26099313
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2607AD24769C794F26CA40E11F73F6AD57957BE613F06B06B445803C17797E45D2E38D24639678360B4CCDF9A8FFF6C1