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DESCRIBE <http://purl.uniprot.org/SHA-384/93D1C5B777F8114A8F417D39FF5206B1A52290031F5EA0840606827CB4298AB687C8669D6A57E589327022B39A942E3A>
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http://purl.uniprot.org/SHA-384/93D1C5B777F8114A8F417D39FF5206B1A52290031F5EA0840606827CB4298AB687C8669D6A57E589327022B39A942E3A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/93D1C5B777F8114A8F417D39FF5206B1A52290031F5EA0840606827CB4298AB687C8669D6A57E589327022B39A942E3A
http://www.w3.org/2000/01/rdf-schema#comment
"Case suggests that SCN2A mutations might predispose children to repetitive encephalopathy with variable clinical and imaging findings."
xsd:string
http://purl.uniprot.org/uniprot/#_F323C595E5C806408DAD7E700A42240AAC5D6C0392BDB567A2649C12CBF02A51AD89CC410F063B67C05AADC0323B59E8
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/93D1C5B777F8114A8F417D39FF5206B1A52290031F5EA0840606827CB4298AB687C8669D6A57E589327022B39A942E3A
http://purl.uniprot.org/uniprot/A8K0U1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/93D1C5B777F8114A8F417D39FF5206B1A52290031F5EA0840606827CB4298AB687C8669D6A57E589327022B39A942E3A
http://purl.uniprot.org/uniprot/#_A8K0U1-mappedCitation-25457084
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/93D1C5B777F8114A8F417D39FF5206B1A52290031F5EA0840606827CB4298AB687C8669D6A57E589327022B39A942E3A