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DESCRIBE <http://purl.uniprot.org/SHA-384/EF7466D37533C990EB004FD202C499C2B30D1CAA4857FA457F67C60F34D95AF769472512CE0C14783361367A37A24324>
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http://purl.uniprot.org/SHA-384/EF7466D37533C990EB004FD202C499C2B30D1CAA4857FA457F67C60F34D95AF769472512CE0C14783361367A37A24324
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EF7466D37533C990EB004FD202C499C2B30D1CAA4857FA457F67C60F34D95AF769472512CE0C14783361367A37A24324
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/#_D0592054DA9DDB5D9181C3FAEB0DF49CCC15D9BA22B4B70A34995BE75302324BEFEFF3BDCDEF1D0F4F287C17A40CC3EC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EF7466D37533C990EB004FD202C499C2B30D1CAA4857FA457F67C60F34D95AF769472512CE0C14783361367A37A24324
http://purl.uniprot.org/uniprot/Q9Y3W7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EF7466D37533C990EB004FD202C499C2B30D1CAA4857FA457F67C60F34D95AF769472512CE0C14783361367A37A24324
http://purl.uniprot.org/uniprot/#_Q9Y3W7-mappedCitation-25600065
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EF7466D37533C990EB004FD202C499C2B30D1CAA4857FA457F67C60F34D95AF769472512CE0C14783361367A37A24324