SPARQL
Downloads
Documentation/Help
Skip Header
Results
Your Query
Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/5B0004CACB31CD4CB9150D09A4BB2F7B916B2F376492539246F63B8B87FDB010817E36961C4C99EE12C381A7C3629482>
Submit Query
Cancel
RDF/XML
NTriples
Turtle
Show query
Share
Subject
Predicate
Object
http://purl.uniprot.org/SHA-384/5B0004CACB31CD4CB9150D09A4BB2F7B916B2F376492539246F63B8B87FDB010817E36961C4C99EE12C381A7C3629482
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5B0004CACB31CD4CB9150D09A4BB2F7B916B2F376492539246F63B8B87FDB010817E36961C4C99EE12C381A7C3629482
http://www.w3.org/2000/01/rdf-schema#comment
"This report provides the first genetic evidence of SCN1B mutation causing the Benign Familial Infantile Epilepsy (BFIE) phenotype."
xsd:string
http://purl.uniprot.org/uniprot/#_177DEDCB137AEB805029558B7D522AF60039FDFD40806CD6F91CE8D2CD1CE659842B5210133C4944F416E1BD42C9A811
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5B0004CACB31CD4CB9150D09A4BB2F7B916B2F376492539246F63B8B87FDB010817E36961C4C99EE12C381A7C3629482
http://purl.uniprot.org/uniprot/Q2KHR9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5B0004CACB31CD4CB9150D09A4BB2F7B916B2F376492539246F63B8B87FDB010817E36961C4C99EE12C381A7C3629482
http://purl.uniprot.org/uniprot/#_Q2KHR9-mappedCitation-28566192
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5B0004CACB31CD4CB9150D09A4BB2F7B916B2F376492539246F63B8B87FDB010817E36961C4C99EE12C381A7C3629482