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DESCRIBE <http://purl.uniprot.org/SHA-384/9B514486D40446B1A08493E1E91441209AED975960AD08A84F440F3A9062DC19468148EFC526980528399266C50CBC24>
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http://purl.uniprot.org/SHA-384/9B514486D40446B1A08493E1E91441209AED975960AD08A84F440F3A9062DC19468148EFC526980528399266C50CBC24
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9B514486D40446B1A08493E1E91441209AED975960AD08A84F440F3A9062DC19468148EFC526980528399266C50CBC24
http://www.w3.org/2000/01/rdf-schema#comment
"Autosomal recessive inheritance and GLK deficiency are features typical for an inborn error of metabolism which occurred in the glucose-insulin signaling pathway in these subjects."
xsd:string
http://purl.uniprot.org/uniprot/#_66E0513BDEDEC4DB4FDC8982EDD981A664A51B999F23045E95C4DB3E80EC923FC99ED60519AFCDA7947F70EB0FC60281
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9B514486D40446B1A08493E1E91441209AED975960AD08A84F440F3A9062DC19468148EFC526980528399266C50CBC24
http://purl.uniprot.org/uniprot/P35557
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9B514486D40446B1A08493E1E91441209AED975960AD08A84F440F3A9062DC19468148EFC526980528399266C50CBC24
http://purl.uniprot.org/uniprot/#_P35557-mappedCitation-14578306
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9B514486D40446B1A08493E1E91441209AED975960AD08A84F440F3A9062DC19468148EFC526980528399266C50CBC24