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DESCRIBE <http://purl.uniprot.org/SHA-384/81A471EADE4E4CB630EE2C880D2BEE9950454FB756E0A6A5D60418066754891E3E9C3924DE397B53E52A571363461207>
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http://purl.uniprot.org/SHA-384/81A471EADE4E4CB630EE2C880D2BEE9950454FB756E0A6A5D60418066754891E3E9C3924DE397B53E52A571363461207
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/81A471EADE4E4CB630EE2C880D2BEE9950454FB756E0A6A5D60418066754891E3E9C3924DE397B53E52A571363461207
http://www.w3.org/2000/01/rdf-schema#comment
"NKX2-1 genetic mutation have been shown to cause cardiac conduction disorders."
xsd:string
http://purl.uniprot.org/uniprot/#_33559D74710E63EB3A90DDAF3943F83A357F7167A8141A42B2C78CD093696EABED6BC0C19D7CCDD7FA8A2CD099BE87BE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/81A471EADE4E4CB630EE2C880D2BEE9950454FB756E0A6A5D60418066754891E3E9C3924DE397B53E52A571363461207
http://purl.uniprot.org/uniprot/P43699
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/81A471EADE4E4CB630EE2C880D2BEE9950454FB756E0A6A5D60418066754891E3E9C3924DE397B53E52A571363461207
http://purl.uniprot.org/uniprot/#_P43699-mappedCitation-25426816
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/81A471EADE4E4CB630EE2C880D2BEE9950454FB756E0A6A5D60418066754891E3E9C3924DE397B53E52A571363461207