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DESCRIBE <http://purl.uniprot.org/SHA-384/070DDB02588C500C64657FB3E84182E04E63620B504EC62CAD8D1281FD29DA58FFB4BE67852CDFB96E9B843B60028040>
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http://purl.uniprot.org/SHA-384/070DDB02588C500C64657FB3E84182E04E63620B504EC62CAD8D1281FD29DA58FFB4BE67852CDFB96E9B843B60028040
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/070DDB02588C500C64657FB3E84182E04E63620B504EC62CAD8D1281FD29DA58FFB4BE67852CDFB96E9B843B60028040
http://www.w3.org/2000/01/rdf-schema#comment
"A novel missense mutation within EIF2B4 is associated with vanishing white matter disease."
xsd:string
http://purl.uniprot.org/uniprot/#_DF3C5FC335E0EABB2AF513096B77CC0EB233CA709EA5CCA165865565AA9F1DAB022DF4C78CDEE6931D5C517ADA6D1451
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/070DDB02588C500C64657FB3E84182E04E63620B504EC62CAD8D1281FD29DA58FFB4BE67852CDFB96E9B843B60028040
http://purl.uniprot.org/uniprot/E7ERK9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/070DDB02588C500C64657FB3E84182E04E63620B504EC62CAD8D1281FD29DA58FFB4BE67852CDFB96E9B843B60028040
http://purl.uniprot.org/uniprot/#_E7ERK9-mappedCitation-25600065
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/070DDB02588C500C64657FB3E84182E04E63620B504EC62CAD8D1281FD29DA58FFB4BE67852CDFB96E9B843B60028040