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DESCRIBE <http://purl.uniprot.org/SHA-384/210D0A481D3778FC21BE7825951F86550CDB7D5892C5247A8805D59037CEFE3968BDB181C9826A7A7326F951312F6293>
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http://purl.uniprot.org/SHA-384/210D0A481D3778FC21BE7825951F86550CDB7D5892C5247A8805D59037CEFE3968BDB181C9826A7A7326F951312F6293
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/210D0A481D3778FC21BE7825951F86550CDB7D5892C5247A8805D59037CEFE3968BDB181C9826A7A7326F951312F6293
http://www.w3.org/2000/01/rdf-schema#comment
"CACNA1B mutation is linked to unique myoclonus-dystonia syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_79EC512E1378F4FF2DD0A7B5DEA1331BF7FCE62A8C3BB49CD624663A9DC88B47FCD03FF04DC047191A07C4CD2E835496
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/210D0A481D3778FC21BE7825951F86550CDB7D5892C5247A8805D59037CEFE3968BDB181C9826A7A7326F951312F6293
http://purl.uniprot.org/uniprot/Q9HBH4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/210D0A481D3778FC21BE7825951F86550CDB7D5892C5247A8805D59037CEFE3968BDB181C9826A7A7326F951312F6293
http://purl.uniprot.org/uniprot/#_Q9HBH4-mappedCitation-25296916
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/210D0A481D3778FC21BE7825951F86550CDB7D5892C5247A8805D59037CEFE3968BDB181C9826A7A7326F951312F6293