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DESCRIBE <http://purl.uniprot.org/SHA-384/B9904B0BC5EA8822C5DC99D073747C09CEBD66A9AFCCC5EF18779011699E7B6B4B318F49D0489C8A600ECEC7A26A9045>
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http://purl.uniprot.org/SHA-384/B9904B0BC5EA8822C5DC99D073747C09CEBD66A9AFCCC5EF18779011699E7B6B4B318F49D0489C8A600ECEC7A26A9045
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B9904B0BC5EA8822C5DC99D073747C09CEBD66A9AFCCC5EF18779011699E7B6B4B318F49D0489C8A600ECEC7A26A9045
http://www.w3.org/2000/01/rdf-schema#comment
"SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome"
xsd:string
http://purl.uniprot.org/uniprot/#_2944509A8D838590292753D17CE68030FBC0F7923E6E89C7B06955E208A2EBF85B0A97B15E3F267983D07EB1E96DEE22
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B9904B0BC5EA8822C5DC99D073747C09CEBD66A9AFCCC5EF18779011699E7B6B4B318F49D0489C8A600ECEC7A26A9045
http://purl.uniprot.org/uniprot/B3KU71
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B9904B0BC5EA8822C5DC99D073747C09CEBD66A9AFCCC5EF18779011699E7B6B4B318F49D0489C8A600ECEC7A26A9045
http://purl.uniprot.org/uniprot/#_B3KU71-mappedCitation-22848613
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B9904B0BC5EA8822C5DC99D073747C09CEBD66A9AFCCC5EF18779011699E7B6B4B318F49D0489C8A600ECEC7A26A9045