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DESCRIBE <http://purl.uniprot.org/SHA-384/7027C7C659076175F76B01F3CD8CF820B55FC76E5136047E0C92D54A2CBE001AC2FE99843B3D1D105AFD39EA7CD862D7>
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http://purl.uniprot.org/SHA-384/7027C7C659076175F76B01F3CD8CF820B55FC76E5136047E0C92D54A2CBE001AC2FE99843B3D1D105AFD39EA7CD862D7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7027C7C659076175F76B01F3CD8CF820B55FC76E5136047E0C92D54A2CBE001AC2FE99843B3D1D105AFD39EA7CD862D7
http://www.w3.org/2000/01/rdf-schema#comment
"Human ADA apart from reducing the adenosine concentration and thus preventing A(1)R desensitization binds to A(1)R behaving as an allosteric effector that markedly enhances agonist affinity and increases receptor functionality."
xsd:string
http://purl.uniprot.org/uniprot/#_B0EEFC9573F36969F13843AC3B85E5DE3C7933FE6DF45132BAB1B6BF261B110C43E4783641CE441310353F181586F950
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7027C7C659076175F76B01F3CD8CF820B55FC76E5136047E0C92D54A2CBE001AC2FE99843B3D1D105AFD39EA7CD862D7
http://purl.uniprot.org/uniprot/P00813
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7027C7C659076175F76B01F3CD8CF820B55FC76E5136047E0C92D54A2CBE001AC2FE99843B3D1D105AFD39EA7CD862D7
http://purl.uniprot.org/uniprot/#_P00813-mappedCitation-18680557
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7027C7C659076175F76B01F3CD8CF820B55FC76E5136047E0C92D54A2CBE001AC2FE99843B3D1D105AFD39EA7CD862D7