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DESCRIBE <http://purl.uniprot.org/SHA-384/7B7FF06DE2BF987C0ABBA02E45F895687EA9BC5DDC41403A5DE4582B44DFA4CC6BE8E0214C5AD8BBD70CCBA4B67F7EC7>
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http://purl.uniprot.org/SHA-384/7B7FF06DE2BF987C0ABBA02E45F895687EA9BC5DDC41403A5DE4582B44DFA4CC6BE8E0214C5AD8BBD70CCBA4B67F7EC7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7B7FF06DE2BF987C0ABBA02E45F895687EA9BC5DDC41403A5DE4582B44DFA4CC6BE8E0214C5AD8BBD70CCBA4B67F7EC7
http://www.w3.org/2000/01/rdf-schema#comment
"Complex I deficiency due to NDUFAF4 mutations causes severe mitochondrial dysfunction and is associated to early death and dysmorphia."
xsd:string
http://purl.uniprot.org/uniprot/#_E835A4A500BEA623ECDCA0C95D234926F8C2AD664261BAE24E015FABF0A84C94FE684576BA37093819AD3F27A47AD729
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7B7FF06DE2BF987C0ABBA02E45F895687EA9BC5DDC41403A5DE4582B44DFA4CC6BE8E0214C5AD8BBD70CCBA4B67F7EC7
http://purl.uniprot.org/uniprot/Q9P032
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7B7FF06DE2BF987C0ABBA02E45F895687EA9BC5DDC41403A5DE4582B44DFA4CC6BE8E0214C5AD8BBD70CCBA4B67F7EC7
http://purl.uniprot.org/uniprot/#_Q9P032-mappedCitation-32949790
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7B7FF06DE2BF987C0ABBA02E45F895687EA9BC5DDC41403A5DE4582B44DFA4CC6BE8E0214C5AD8BBD70CCBA4B67F7EC7