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DESCRIBE <http://purl.uniprot.org/SHA-384/A700399D70520B8FA02FFD155BA34D65736DCF0C525B179E666590B6FA6DAC8FA09F77236D67F27C34664CE6FF93DE3A>
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http://purl.uniprot.org/SHA-384/A700399D70520B8FA02FFD155BA34D65736DCF0C525B179E666590B6FA6DAC8FA09F77236D67F27C34664CE6FF93DE3A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A700399D70520B8FA02FFD155BA34D65736DCF0C525B179E666590B6FA6DAC8FA09F77236D67F27C34664CE6FF93DE3A
http://www.w3.org/2000/01/rdf-schema#comment
"Heterozygous mutations in the DUOX2 gene are responsible for iodide organification defect and congenital hypothyroidism."
xsd:string
http://purl.uniprot.org/uniprot/#_D5B9EF9997F7A150BB1839D0518807833F879B9A217BDBCA33FC11ABE31CC589FB61A9439B14C3B751126427C16CEF49
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A700399D70520B8FA02FFD155BA34D65736DCF0C525B179E666590B6FA6DAC8FA09F77236D67F27C34664CE6FF93DE3A
http://purl.uniprot.org/uniprot/A0A0A8J1J7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A700399D70520B8FA02FFD155BA34D65736DCF0C525B179E666590B6FA6DAC8FA09F77236D67F27C34664CE6FF93DE3A
http://purl.uniprot.org/uniprot/#_A0A0A8J1J7-mappedCitation-16322276
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A700399D70520B8FA02FFD155BA34D65736DCF0C525B179E666590B6FA6DAC8FA09F77236D67F27C34664CE6FF93DE3A