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DESCRIBE <http://purl.uniprot.org/SHA-384/0ED8E453495181BB12807F1C6414B7CBCD000387DA5BB786DF727A601039F78F36F5961673301B921C41BF65907EE26E>
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http://purl.uniprot.org/SHA-384/0ED8E453495181BB12807F1C6414B7CBCD000387DA5BB786DF727A601039F78F36F5961673301B921C41BF65907EE26E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0ED8E453495181BB12807F1C6414B7CBCD000387DA5BB786DF727A601039F78F36F5961673301B921C41BF65907EE26E
http://www.w3.org/2000/01/rdf-schema#comment
"These data suggest that individuals with an SLC26A4 single-allele mutation combined with FOXI1 or KCNJ10 gene mutations do not suffer hearing loss during infancy"
xsd:string
http://purl.uniprot.org/uniprot/#_8F0F7A2D6EE47EDBD6B2C57DAF421BDAD39B890455DA0E2613534AB4ED563F359079142D6F5EAFCB19221638A340F26D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/0ED8E453495181BB12807F1C6414B7CBCD000387DA5BB786DF727A601039F78F36F5961673301B921C41BF65907EE26E
http://purl.uniprot.org/uniprot/E0XEN6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0ED8E453495181BB12807F1C6414B7CBCD000387DA5BB786DF727A601039F78F36F5961673301B921C41BF65907EE26E
http://purl.uniprot.org/uniprot/#_E0XEN6-mappedCitation-31243244
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0ED8E453495181BB12807F1C6414B7CBCD000387DA5BB786DF727A601039F78F36F5961673301B921C41BF65907EE26E