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DESCRIBE <http://purl.uniprot.org/SHA-384/A5A9243E7E03B2DAF6270277A7A764523CF8C6904320C2D3E5568B593A11AC9D0E544C479EC04E3F9B3B1A8294B3E994>
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http://purl.uniprot.org/SHA-384/A5A9243E7E03B2DAF6270277A7A764523CF8C6904320C2D3E5568B593A11AC9D0E544C479EC04E3F9B3B1A8294B3E994
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A5A9243E7E03B2DAF6270277A7A764523CF8C6904320C2D3E5568B593A11AC9D0E544C479EC04E3F9B3B1A8294B3E994
http://www.w3.org/2000/01/rdf-schema#comment
"This report represents the first example of SDHB mutation as a cause of inherited mitochondrial respiratory chain disease and extends the SDHA mutation spectrum in patients with isolated complex II deficiency."
xsd:string
http://purl.uniprot.org/uniprot/#_85D1AA8AA8B303D989CC12E59DD94F581B37485FBDA1225C61E483459E28E7E1416EDCFAFC29D64218AB19FE591D1DE6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A5A9243E7E03B2DAF6270277A7A764523CF8C6904320C2D3E5568B593A11AC9D0E544C479EC04E3F9B3B1A8294B3E994
http://purl.uniprot.org/uniprot/B4DYN5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A5A9243E7E03B2DAF6270277A7A764523CF8C6904320C2D3E5568B593A11AC9D0E544C479EC04E3F9B3B1A8294B3E994
http://purl.uniprot.org/uniprot/#_B4DYN5-mappedCitation-22972948
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A5A9243E7E03B2DAF6270277A7A764523CF8C6904320C2D3E5568B593A11AC9D0E544C479EC04E3F9B3B1A8294B3E994