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DESCRIBE <http://purl.uniprot.org/SHA-384/AF79A041253A33200A2A7D302A64E4847D7E3BBCEAABD094E658242DFC63EAAD57D572ABDAF4FDC6AE8C06FED9939438>
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http://purl.uniprot.org/SHA-384/AF79A041253A33200A2A7D302A64E4847D7E3BBCEAABD094E658242DFC63EAAD57D572ABDAF4FDC6AE8C06FED9939438
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/AF79A041253A33200A2A7D302A64E4847D7E3BBCEAABD094E658242DFC63EAAD57D572ABDAF4FDC6AE8C06FED9939438
http://www.w3.org/2000/01/rdf-schema#comment
"Two novel mutations in the SCNN1A gene causing pseudohypoaldosteronism type 1 have been identified in two unrelated Chinese infants."
xsd:string
http://purl.uniprot.org/uniprot/#_8383545F325A1898B60790B417676F8ACFFD5294D1326D46B2814A49443A071C94DF6ED63A827E4D6BE2DBC447D8365D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/AF79A041253A33200A2A7D302A64E4847D7E3BBCEAABD094E658242DFC63EAAD57D572ABDAF4FDC6AE8C06FED9939438
http://purl.uniprot.org/uniprot/P37088
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AF79A041253A33200A2A7D302A64E4847D7E3BBCEAABD094E658242DFC63EAAD57D572ABDAF4FDC6AE8C06FED9939438
http://purl.uniprot.org/uniprot/#_P37088-mappedCitation-23762408
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AF79A041253A33200A2A7D302A64E4847D7E3BBCEAABD094E658242DFC63EAAD57D572ABDAF4FDC6AE8C06FED9939438