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DESCRIBE <http://purl.uniprot.org/SHA-384/6409BE0727C99B289FD8864268BC5ACF6794F719D31E3411EEBE68CBE168976466D0A6FFA390246DF33FF6CD6C7D430C>
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http://purl.uniprot.org/SHA-384/6409BE0727C99B289FD8864268BC5ACF6794F719D31E3411EEBE68CBE168976466D0A6FFA390246DF33FF6CD6C7D430C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6409BE0727C99B289FD8864268BC5ACF6794F719D31E3411EEBE68CBE168976466D0A6FFA390246DF33FF6CD6C7D430C
http://www.w3.org/2000/01/rdf-schema#comment
"DUOX2 Mutation is associated with Congenital Hypothyroidism."
xsd:string
http://purl.uniprot.org/uniprot/#_6DD98156727ADC46B2A55C6FC39B29B9DC89A4CEED99256400714F6DC9504E3269EF6F18EA94B44D3CE5B137514393E3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6409BE0727C99B289FD8864268BC5ACF6794F719D31E3411EEBE68CBE168976466D0A6FFA390246DF33FF6CD6C7D430C
http://purl.uniprot.org/uniprot/A0A0A8J1J7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6409BE0727C99B289FD8864268BC5ACF6794F719D31E3411EEBE68CBE168976466D0A6FFA390246DF33FF6CD6C7D430C
http://purl.uniprot.org/uniprot/#_A0A0A8J1J7-mappedCitation-27557340
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6409BE0727C99B289FD8864268BC5ACF6794F719D31E3411EEBE68CBE168976466D0A6FFA390246DF33FF6CD6C7D430C