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DESCRIBE <http://purl.uniprot.org/SHA-384/B811042273592B2C29CA8D7E3D304445E230D14E8F4206292E7FAF897FE38AAA6E392B2CF25660B047F81FD58D376A48>
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http://purl.uniprot.org/SHA-384/B811042273592B2C29CA8D7E3D304445E230D14E8F4206292E7FAF897FE38AAA6E392B2CF25660B047F81FD58D376A48
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B811042273592B2C29CA8D7E3D304445E230D14E8F4206292E7FAF897FE38AAA6E392B2CF25660B047F81FD58D376A48
http://www.w3.org/2000/01/rdf-schema#comment
"Late-onset manifestation of Bartter syndrome resulted from residual function of the mutated renal SLC12A1."
xsd:string
http://purl.uniprot.org/uniprot/#_299145F9B3535CA9A7A40C3DD0A570A4C5D7B5E97E80EED2E80B4BCB1631179051A39C70CE0D0EC50FA6D3D1D1570904
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B811042273592B2C29CA8D7E3D304445E230D14E8F4206292E7FAF897FE38AAA6E392B2CF25660B047F81FD58D376A48
http://purl.uniprot.org/uniprot/Q8IUN5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B811042273592B2C29CA8D7E3D304445E230D14E8F4206292E7FAF897FE38AAA6E392B2CF25660B047F81FD58D376A48
http://purl.uniprot.org/uniprot/#_Q8IUN5-mappedCitation-16807401
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B811042273592B2C29CA8D7E3D304445E230D14E8F4206292E7FAF897FE38AAA6E392B2CF25660B047F81FD58D376A48