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DESCRIBE <http://purl.uniprot.org/SHA-384/58F044975154FA4FF7CE3B91491AF0F2DE5C6085FF6DAC03102AD51E2F15B8F0056895C3B2AB60DCEAA4066840B53E4F>
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http://purl.uniprot.org/SHA-384/58F044975154FA4FF7CE3B91491AF0F2DE5C6085FF6DAC03102AD51E2F15B8F0056895C3B2AB60DCEAA4066840B53E4F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/58F044975154FA4FF7CE3B91491AF0F2DE5C6085FF6DAC03102AD51E2F15B8F0056895C3B2AB60DCEAA4066840B53E4F
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations of COX15 causing single amino acid conversions are associated with fatal infantile hypertrophic cardiomyopathy and the neurological disorder Leigh syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_8B99D80216D810D3595C06941A5ABAF7C0905A2A418348EB53F8ABF7CE97F76C760DB01A88166BFCB41854FAFB8D91CE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/58F044975154FA4FF7CE3B91491AF0F2DE5C6085FF6DAC03102AD51E2F15B8F0056895C3B2AB60DCEAA4066840B53E4F
http://purl.uniprot.org/uniprot/Q7KZN9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/58F044975154FA4FF7CE3B91491AF0F2DE5C6085FF6DAC03102AD51E2F15B8F0056895C3B2AB60DCEAA4066840B53E4F
http://purl.uniprot.org/uniprot/#_Q7KZN9-mappedCitation-26940873
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/58F044975154FA4FF7CE3B91491AF0F2DE5C6085FF6DAC03102AD51E2F15B8F0056895C3B2AB60DCEAA4066840B53E4F