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DESCRIBE <http://purl.uniprot.org/SHA-384/AE4878A9015E3A7A7A329B96A5F4C23E99000295372E22819D90887AADAD068CD6880A4D38952325D3448E65DFC1CEA2>
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http://purl.uniprot.org/SHA-384/AE4878A9015E3A7A7A329B96A5F4C23E99000295372E22819D90887AADAD068CD6880A4D38952325D3448E65DFC1CEA2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/AE4878A9015E3A7A7A329B96A5F4C23E99000295372E22819D90887AADAD068CD6880A4D38952325D3448E65DFC1CEA2
http://www.w3.org/2000/01/rdf-schema#comment
"The majority of mutations responsible for autosomatic dominant optic atrophy are localized in OPA1 gene."
xsd:string
http://purl.uniprot.org/uniprot/#_251C41339EA9741BA575B1F9F0F0A158AB5AA0D6F6E7C16B574EBDF98AC26ADB57A42B7E7AB9DFC7F846CC080F100FA6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/AE4878A9015E3A7A7A329B96A5F4C23E99000295372E22819D90887AADAD068CD6880A4D38952325D3448E65DFC1CEA2
http://purl.uniprot.org/uniprot/E5KLK0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AE4878A9015E3A7A7A329B96A5F4C23E99000295372E22819D90887AADAD068CD6880A4D38952325D3448E65DFC1CEA2
http://purl.uniprot.org/uniprot/#_E5KLK0-mappedCitation-18488399
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AE4878A9015E3A7A7A329B96A5F4C23E99000295372E22819D90887AADAD068CD6880A4D38952325D3448E65DFC1CEA2