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DESCRIBE <http://purl.uniprot.org/SHA-384/E0F05BEFF72C182C598EF80EA8D4CBC092AF1C1BECD60594184E3CD0D24B92924B4151BFF24708FDA7C44A0DB8F7C102>
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http://purl.uniprot.org/SHA-384/E0F05BEFF72C182C598EF80EA8D4CBC092AF1C1BECD60594184E3CD0D24B92924B4151BFF24708FDA7C44A0DB8F7C102
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E0F05BEFF72C182C598EF80EA8D4CBC092AF1C1BECD60594184E3CD0D24B92924B4151BFF24708FDA7C44A0DB8F7C102
http://www.w3.org/2000/01/rdf-schema#comment
"Pathogenicity of the human truncation mutant results from its inability to sequester adenosyltransferase (AdoCbl) for direct transfer to methylmalonyl-CoA mutase resulting in holoenzyme formation and disease."
xsd:string
http://purl.uniprot.org/uniprot/#_90424322A275289A37219DC7249EAC8F3A7F0D149944E04C955A1C584C89F14AD50C24131AE4199F3377271E79F39148
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E0F05BEFF72C182C598EF80EA8D4CBC092AF1C1BECD60594184E3CD0D24B92924B4151BFF24708FDA7C44A0DB8F7C102
http://purl.uniprot.org/uniprot/Q59HB4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E0F05BEFF72C182C598EF80EA8D4CBC092AF1C1BECD60594184E3CD0D24B92924B4151BFF24708FDA7C44A0DB8F7C102
http://purl.uniprot.org/uniprot/#_Q59HB4-mappedCitation-21604717
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E0F05BEFF72C182C598EF80EA8D4CBC092AF1C1BECD60594184E3CD0D24B92924B4151BFF24708FDA7C44A0DB8F7C102