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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/0E8A6D78149DD8569BC0565BC2F4BF879494809435D1A2821BC6A15E3AB2DDA9C501B74934E559E7DDBEAE7E74298196>
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http://purl.uniprot.org/SHA-384/0E8A6D78149DD8569BC0565BC2F4BF879494809435D1A2821BC6A15E3AB2DDA9C501B74934E559E7DDBEAE7E74298196
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0E8A6D78149DD8569BC0565BC2F4BF879494809435D1A2821BC6A15E3AB2DDA9C501B74934E559E7DDBEAE7E74298196
http://www.w3.org/2000/01/rdf-schema#comment
"The R445H mutation in OPA1 might be the cause of the association between dominant optic atrophy and moderate deafness a phenotype that may be currently underdiagnosed."
xsd:string
http://purl.uniprot.org/uniprot/#_E2BBC45207282CD9A2657E761AAF0C552A3346515987EDD85C35989A0219A0E3515288FB55287FA7F81F9DDE4BA27F10
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/0E8A6D78149DD8569BC0565BC2F4BF879494809435D1A2821BC6A15E3AB2DDA9C501B74934E559E7DDBEAE7E74298196
http://purl.uniprot.org/uniprot/E5KLJ9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0E8A6D78149DD8569BC0565BC2F4BF879494809435D1A2821BC6A15E3AB2DDA9C501B74934E559E7DDBEAE7E74298196
http://purl.uniprot.org/uniprot/#_E5KLJ9-mappedCitation-14644237
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0E8A6D78149DD8569BC0565BC2F4BF879494809435D1A2821BC6A15E3AB2DDA9C501B74934E559E7DDBEAE7E74298196