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DESCRIBE <http://purl.uniprot.org/SHA-384/EDF7D241A2B52F6B39ED335EB2D3FFF5C74E7D65141AE29F1A3A72CC69897D6CA35A795314351691FE8F899358930FB5>
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http://purl.uniprot.org/SHA-384/EDF7D241A2B52F6B39ED335EB2D3FFF5C74E7D65141AE29F1A3A72CC69897D6CA35A795314351691FE8F899358930FB5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EDF7D241A2B52F6B39ED335EB2D3FFF5C74E7D65141AE29F1A3A72CC69897D6CA35A795314351691FE8F899358930FB5
http://www.w3.org/2000/01/rdf-schema#comment
"The phenotypic spectrum in grin2a mutations ranged from normal or near-normal development with mild epilepsy and speech delay/apraxia to severe developmental and epileptic encephalopathy often within the epilepsy-aphasia spectrum."
xsd:string
http://purl.uniprot.org/uniprot/#_5579BFEC43CBCAFC90229A06D0C97060F80686099A3CE8015419755D8D4650AF2FB7DCD62B223E2468C1470A6CC7C8BB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EDF7D241A2B52F6B39ED335EB2D3FFF5C74E7D65141AE29F1A3A72CC69897D6CA35A795314351691FE8F899358930FB5
http://purl.uniprot.org/uniprot/Q547U9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EDF7D241A2B52F6B39ED335EB2D3FFF5C74E7D65141AE29F1A3A72CC69897D6CA35A795314351691FE8F899358930FB5
http://purl.uniprot.org/uniprot/#_Q547U9-mappedCitation-30544257
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EDF7D241A2B52F6B39ED335EB2D3FFF5C74E7D65141AE29F1A3A72CC69897D6CA35A795314351691FE8F899358930FB5