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DESCRIBE <http://purl.uniprot.org/SHA-384/AC751DCC1B0605AB8804743DBC451AAC311C3F74132437982E66452EC47AFE8D8626F2E1C3E78509466EE9123D910492>
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http://purl.uniprot.org/SHA-384/AC751DCC1B0605AB8804743DBC451AAC311C3F74132437982E66452EC47AFE8D8626F2E1C3E78509466EE9123D910492
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/AC751DCC1B0605AB8804743DBC451AAC311C3F74132437982E66452EC47AFE8D8626F2E1C3E78509466EE9123D910492
http://www.w3.org/2000/01/rdf-schema#comment
"These results suggested that the functional defect of novel truncated HNF-1alpha (G554fsX556) on the transactivation of its target-gene promoters would account for the beta-cell dysfunction associated with the pathogenesis of MODY"
xsd:string
http://purl.uniprot.org/uniprot/#_D627D11E8600C1A5355B2F77B8357D5DF9B49D5A7D787240B2F197AA5F6AD6FDE9F5858A31DC40D117E88AD561926611
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/AC751DCC1B0605AB8804743DBC451AAC311C3F74132437982E66452EC47AFE8D8626F2E1C3E78509466EE9123D910492
http://purl.uniprot.org/uniprot/Q90867
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AC751DCC1B0605AB8804743DBC451AAC311C3F74132437982E66452EC47AFE8D8626F2E1C3E78509466EE9123D910492
http://purl.uniprot.org/uniprot/#_Q90867-mappedCitation-19336222
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AC751DCC1B0605AB8804743DBC451AAC311C3F74132437982E66452EC47AFE8D8626F2E1C3E78509466EE9123D910492