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DESCRIBE <http://purl.uniprot.org/SHA-384/94BA553C389EA6491C0F8C3E54D94F8B7B97676AC6608ECEB9A09622E06A794F17EABAE33F10DFE82C1EA13DB5F79F0E>
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http://purl.uniprot.org/SHA-384/94BA553C389EA6491C0F8C3E54D94F8B7B97676AC6608ECEB9A09622E06A794F17EABAE33F10DFE82C1EA13DB5F79F0E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/94BA553C389EA6491C0F8C3E54D94F8B7B97676AC6608ECEB9A09622E06A794F17EABAE33F10DFE82C1EA13DB5F79F0E
http://www.w3.org/2000/01/rdf-schema#comment
"We describe the first Chinese patient with typical clinical and radiological features genetically confirmed to have vanishing white matter disease for a mutation in EIF2B4."
xsd:string
http://purl.uniprot.org/uniprot/#_08C6FD184519439E85598CED9726471E6A2C38462AC5A1AE0AE51DBDB1AA65A87F190C0E1FEC172057335B808D4EB736
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/94BA553C389EA6491C0F8C3E54D94F8B7B97676AC6608ECEB9A09622E06A794F17EABAE33F10DFE82C1EA13DB5F79F0E
http://purl.uniprot.org/uniprot/Q9Y3W7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/94BA553C389EA6491C0F8C3E54D94F8B7B97676AC6608ECEB9A09622E06A794F17EABAE33F10DFE82C1EA13DB5F79F0E
http://purl.uniprot.org/uniprot/#_Q9Y3W7-mappedCitation-18539998
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/94BA553C389EA6491C0F8C3E54D94F8B7B97676AC6608ECEB9A09622E06A794F17EABAE33F10DFE82C1EA13DB5F79F0E