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DESCRIBE <http://purl.uniprot.org/SHA-384/9AAEC0967BBBE8B8D82A23D77481A640DA6157FC4D3B8E88DB51557911DEC0C40814D516490AF3B048B4091251FDBE1E>
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http://purl.uniprot.org/SHA-384/9AAEC0967BBBE8B8D82A23D77481A640DA6157FC4D3B8E88DB51557911DEC0C40814D516490AF3B048B4091251FDBE1E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9AAEC0967BBBE8B8D82A23D77481A640DA6157FC4D3B8E88DB51557911DEC0C40814D516490AF3B048B4091251FDBE1E
http://www.w3.org/2000/01/rdf-schema#comment
"exon-skipping variants form heteromeric complexes with EAAT2wt or EAAT2b that traffic to the membrane but show reduced glutamate-dependent activity. This could allow glutamate to accumulate extracellularly and promote excitotoxicity."
xsd:string
http://purl.uniprot.org/uniprot/#_206F35B6DBF56CAA7100845133D474E3191E9F6F1745C3FCC1F96534A0F7DEEB7914158BBF34B4EEF4F93719E78947A3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9AAEC0967BBBE8B8D82A23D77481A640DA6157FC4D3B8E88DB51557911DEC0C40814D516490AF3B048B4091251FDBE1E
http://purl.uniprot.org/uniprot/A0A2R8YFE3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9AAEC0967BBBE8B8D82A23D77481A640DA6157FC4D3B8E88DB51557911DEC0C40814D516490AF3B048B4091251FDBE1E
http://purl.uniprot.org/uniprot/#_A0A2R8YFE3-mappedCitation-20688910
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9AAEC0967BBBE8B8D82A23D77481A640DA6157FC4D3B8E88DB51557911DEC0C40814D516490AF3B048B4091251FDBE1E