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DESCRIBE <http://purl.uniprot.org/SHA-384/9CF706D4F51DB2F4C407FCDFC92C1A7D839B0C4CC2CF14A4BD4B689AD75DA0C8025643B1BAD30FB2644721E61DF26968>
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http://purl.uniprot.org/SHA-384/9CF706D4F51DB2F4C407FCDFC92C1A7D839B0C4CC2CF14A4BD4B689AD75DA0C8025643B1BAD30FB2644721E61DF26968
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9CF706D4F51DB2F4C407FCDFC92C1A7D839B0C4CC2CF14A4BD4B689AD75DA0C8025643B1BAD30FB2644721E61DF26968
http://www.w3.org/2000/01/rdf-schema#comment
"Fifty-nine percent of childhood-onset patients with T1DM were identified with high genetic risk based on known HLA-DQA1/B1 associations"
xsd:string
http://purl.uniprot.org/uniprot/#_1EE4E613AE30FDC83EBAAF0F22B1A7E7B6685DB3DCF35F9FF9FB2C8E3A8A7156159DEC9F92A4E65064CB56A2827C1469
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9CF706D4F51DB2F4C407FCDFC92C1A7D839B0C4CC2CF14A4BD4B689AD75DA0C8025643B1BAD30FB2644721E61DF26968
http://purl.uniprot.org/uniprot/Q29995
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9CF706D4F51DB2F4C407FCDFC92C1A7D839B0C4CC2CF14A4BD4B689AD75DA0C8025643B1BAD30FB2644721E61DF26968
http://purl.uniprot.org/uniprot/#_Q29995-mappedCitation-21418452
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9CF706D4F51DB2F4C407FCDFC92C1A7D839B0C4CC2CF14A4BD4B689AD75DA0C8025643B1BAD30FB2644721E61DF26968