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DESCRIBE <http://purl.uniprot.org/SHA-384/F7D07B4B2030BDD25322246756C15D2077D5F18885328852A8F04E863E303889D7CE2DE13953B018F87CC4B157248099>
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http://purl.uniprot.org/SHA-384/F7D07B4B2030BDD25322246756C15D2077D5F18885328852A8F04E863E303889D7CE2DE13953B018F87CC4B157248099
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F7D07B4B2030BDD25322246756C15D2077D5F18885328852A8F04E863E303889D7CE2DE13953B018F87CC4B157248099
http://www.w3.org/2000/01/rdf-schema#comment
"he clinical feature of TBC1D24 gene mutation related epilepsy was focal myoclonus and tended to develop into myoclonic status epilepticus and could be aggravated by infections and terminated by sleep or sedation drugs."
xsd:string
http://purl.uniprot.org/uniprot/#_439C72F1B7BD41E4270F98DF7EE65FF3EBD9AB12EC1E17569D7A0CEBDDCF64B2263C73477CF9B5552D80E1BCD29D50B1
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F7D07B4B2030BDD25322246756C15D2077D5F18885328852A8F04E863E303889D7CE2DE13953B018F87CC4B157248099
http://purl.uniprot.org/uniprot/Q9ULP9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F7D07B4B2030BDD25322246756C15D2077D5F18885328852A8F04E863E303889D7CE2DE13953B018F87CC4B157248099
http://purl.uniprot.org/uniprot/#_Q9ULP9-mappedCitation-30180405
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F7D07B4B2030BDD25322246756C15D2077D5F18885328852A8F04E863E303889D7CE2DE13953B018F87CC4B157248099