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DESCRIBE <http://purl.uniprot.org/SHA-384/DF5A34CFA725EFDE175E95B84F3FE8F531191247BD2737227DF4C5A3AF950009D6156EA390BF11C0EDDF2BA7759903EA>
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http://purl.uniprot.org/SHA-384/DF5A34CFA725EFDE175E95B84F3FE8F531191247BD2737227DF4C5A3AF950009D6156EA390BF11C0EDDF2BA7759903EA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DF5A34CFA725EFDE175E95B84F3FE8F531191247BD2737227DF4C5A3AF950009D6156EA390BF11C0EDDF2BA7759903EA
http://www.w3.org/2000/01/rdf-schema#comment
"Bi-allelic Loss-of-Function CACNA1B Mutations are associated with Progressive Epilepsy-Dyskinesia."
xsd:string
http://purl.uniprot.org/uniprot/#_BB9900AC1EED33CFB835621801D8F9A8D79D66FCA2B3E55A96A27F773C5F8031EBF0D11FC735768B6E1539F75A6B8960
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DF5A34CFA725EFDE175E95B84F3FE8F531191247BD2737227DF4C5A3AF950009D6156EA390BF11C0EDDF2BA7759903EA
http://purl.uniprot.org/uniprot/Q9HAT4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DF5A34CFA725EFDE175E95B84F3FE8F531191247BD2737227DF4C5A3AF950009D6156EA390BF11C0EDDF2BA7759903EA
http://purl.uniprot.org/uniprot/#_Q9HAT4-mappedCitation-30982612
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DF5A34CFA725EFDE175E95B84F3FE8F531191247BD2737227DF4C5A3AF950009D6156EA390BF11C0EDDF2BA7759903EA