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DESCRIBE <http://purl.uniprot.org/SHA-384/44DAD5189BB559696353C0155C9B4CEEDC76B1F61725781753122CF5724DA6DF91A52781B641574D3C6F53E44A2C9AEE>
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http://purl.uniprot.org/SHA-384/44DAD5189BB559696353C0155C9B4CEEDC76B1F61725781753122CF5724DA6DF91A52781B641574D3C6F53E44A2C9AEE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/44DAD5189BB559696353C0155C9B4CEEDC76B1F61725781753122CF5724DA6DF91A52781B641574D3C6F53E44A2C9AEE
http://www.w3.org/2000/01/rdf-schema#comment
"Our data indicate that the LEU396ARG mutation in OPA1 is associated with severe dominant optic atrophy."
xsd:string
http://purl.uniprot.org/uniprot/#_4054883B566C15CC6A013766F5E8BCA27E380E35B026826B8553186B2B80001D48776F20096268C002195E0EC1B321E7
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/44DAD5189BB559696353C0155C9B4CEEDC76B1F61725781753122CF5724DA6DF91A52781B641574D3C6F53E44A2C9AEE
http://purl.uniprot.org/uniprot/E5KLJ9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/44DAD5189BB559696353C0155C9B4CEEDC76B1F61725781753122CF5724DA6DF91A52781B641574D3C6F53E44A2C9AEE
http://purl.uniprot.org/uniprot/#_E5KLJ9-mappedCitation-29350691
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/44DAD5189BB559696353C0155C9B4CEEDC76B1F61725781753122CF5724DA6DF91A52781B641574D3C6F53E44A2C9AEE