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DESCRIBE <http://purl.uniprot.org/SHA-384/7A2316227E69F0DA2D4A7F3976DC4CFB275DD249673B1F63B62952F81CD9EC0CB35CDAE18EA5A82E65FBB9A1FF50AE4D>
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http://purl.uniprot.org/SHA-384/7A2316227E69F0DA2D4A7F3976DC4CFB275DD249673B1F63B62952F81CD9EC0CB35CDAE18EA5A82E65FBB9A1FF50AE4D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7A2316227E69F0DA2D4A7F3976DC4CFB275DD249673B1F63B62952F81CD9EC0CB35CDAE18EA5A82E65FBB9A1FF50AE4D
http://www.w3.org/2000/01/rdf-schema#comment
"GRIN2A mutation is associated with epilepsy-aphasia spectrum disorders but with a relatively low rate."
xsd:string
http://purl.uniprot.org/uniprot/#_A07480B616D371191B3344557A0822A6E058EA12CAC67518AB77AF1248EE3049F681A335D7E0149B91E3B4E4BA07BC30
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7A2316227E69F0DA2D4A7F3976DC4CFB275DD249673B1F63B62952F81CD9EC0CB35CDAE18EA5A82E65FBB9A1FF50AE4D
http://purl.uniprot.org/uniprot/Q59EW6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7A2316227E69F0DA2D4A7F3976DC4CFB275DD249673B1F63B62952F81CD9EC0CB35CDAE18EA5A82E65FBB9A1FF50AE4D
http://purl.uniprot.org/uniprot/#_Q59EW6-mappedCitation-29896722
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7A2316227E69F0DA2D4A7F3976DC4CFB275DD249673B1F63B62952F81CD9EC0CB35CDAE18EA5A82E65FBB9A1FF50AE4D