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DESCRIBE <http://purl.uniprot.org/SHA-384/9FB0EBF1A57FB675F2DC1DD2BA11FEA98B7FDBEAFAE3F94B309A5943D51F748066FBAE455C1C9134CED9FA258535A4A3>
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http://purl.uniprot.org/SHA-384/9FB0EBF1A57FB675F2DC1DD2BA11FEA98B7FDBEAFAE3F94B309A5943D51F748066FBAE455C1C9134CED9FA258535A4A3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9FB0EBF1A57FB675F2DC1DD2BA11FEA98B7FDBEAFAE3F94B309A5943D51F748066FBAE455C1C9134CED9FA258535A4A3
http://www.w3.org/2000/01/rdf-schema#comment
"Revisiting the clinical impact of variants in EFHC1 in patients with different phenotypes of genetic generalized epilepsy."
xsd:string
http://purl.uniprot.org/uniprot/#_B8A3B704EDE59D4E1383D5662EBBA13B11A484F8C430B783CD77D696D4DE207E94D4827F3D994E5C8337FC7B106A9994
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9FB0EBF1A57FB675F2DC1DD2BA11FEA98B7FDBEAFAE3F94B309A5943D51F748066FBAE455C1C9134CED9FA258535A4A3
http://purl.uniprot.org/uniprot/B2CKC5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9FB0EBF1A57FB675F2DC1DD2BA11FEA98B7FDBEAFAE3F94B309A5943D51F748066FBAE455C1C9134CED9FA258535A4A3
http://purl.uniprot.org/uniprot/#_B2CKC5-mappedCitation-33181902
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9FB0EBF1A57FB675F2DC1DD2BA11FEA98B7FDBEAFAE3F94B309A5943D51F748066FBAE455C1C9134CED9FA258535A4A3