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DESCRIBE <http://purl.uniprot.org/SHA-384/A95130DD11946C79AAEE8A223DF865DBC5EA04DB31C5B140AFE8EC4ED5979C7D75355933F784CB848ABC15B7D4909873>
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http://purl.uniprot.org/SHA-384/A95130DD11946C79AAEE8A223DF865DBC5EA04DB31C5B140AFE8EC4ED5979C7D75355933F784CB848ABC15B7D4909873
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A95130DD11946C79AAEE8A223DF865DBC5EA04DB31C5B140AFE8EC4ED5979C7D75355933F784CB848ABC15B7D4909873
http://www.w3.org/2000/01/rdf-schema#comment
"The novel mutation found in this study is a frameshift/deletion at aa 915 in the C-terminal region of hERG that removes a putative assembly domain of the channel protein and is associated with arrythmias and syncope"
xsd:string
http://purl.uniprot.org/uniprot/#_6C1DDEA6DD95E8BA38BCFD7618CCEA2889205E370EB3BCF5D77B927034F00B0D4550DE2C4F787FCC6D6236B9359B19F6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A95130DD11946C79AAEE8A223DF865DBC5EA04DB31C5B140AFE8EC4ED5979C7D75355933F784CB848ABC15B7D4909873
http://purl.uniprot.org/uniprot/A0A090N8Q0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A95130DD11946C79AAEE8A223DF865DBC5EA04DB31C5B140AFE8EC4ED5979C7D75355933F784CB848ABC15B7D4909873
http://purl.uniprot.org/uniprot/#_A0A090N8Q0-mappedCitation-18984536
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A95130DD11946C79AAEE8A223DF865DBC5EA04DB31C5B140AFE8EC4ED5979C7D75355933F784CB848ABC15B7D4909873