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DESCRIBE <http://purl.uniprot.org/SHA-384/599A7DF8B9BA57BE9E8EF233F0852E3F560915671F6136D4AEE8E7D28AC6D78B53FCA6FF8B7F83F4872D562E65517FD8>
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http://purl.uniprot.org/SHA-384/599A7DF8B9BA57BE9E8EF233F0852E3F560915671F6136D4AEE8E7D28AC6D78B53FCA6FF8B7F83F4872D562E65517FD8
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/599A7DF8B9BA57BE9E8EF233F0852E3F560915671F6136D4AEE8E7D28AC6D78B53FCA6FF8B7F83F4872D562E65517FD8
http://www.w3.org/2000/01/rdf-schema#comment
"Mutation in EIF2B4 causes childhood ataxia with central nervous system hypomyelination/ vanishing white matter leukodystrophy."
xsd:string
http://purl.uniprot.org/uniprot/#_42EC071E6869FCBE29C7A2B2D437DAD299059E4ECC2E7FEF10DB809CAE919C77949D444447538C987B9067F379C599DA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/599A7DF8B9BA57BE9E8EF233F0852E3F560915671F6136D4AEE8E7D28AC6D78B53FCA6FF8B7F83F4872D562E65517FD8
http://purl.uniprot.org/uniprot/Q9Y3W7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/599A7DF8B9BA57BE9E8EF233F0852E3F560915671F6136D4AEE8E7D28AC6D78B53FCA6FF8B7F83F4872D562E65517FD8
http://purl.uniprot.org/uniprot/#_Q9Y3W7-mappedCitation-12707859
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/599A7DF8B9BA57BE9E8EF233F0852E3F560915671F6136D4AEE8E7D28AC6D78B53FCA6FF8B7F83F4872D562E65517FD8