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DESCRIBE <http://purl.uniprot.org/SHA-384/2302BBE2C5FCD6A4A10FBA3543098D3C54BB2240D5C2464360344B3B3BE41FB2236FA3B474319D9988DC20411BD6A127>
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http://purl.uniprot.org/SHA-384/2302BBE2C5FCD6A4A10FBA3543098D3C54BB2240D5C2464360344B3B3BE41FB2236FA3B474319D9988DC20411BD6A127
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2302BBE2C5FCD6A4A10FBA3543098D3C54BB2240D5C2464360344B3B3BE41FB2236FA3B474319D9988DC20411BD6A127
http://www.w3.org/2000/01/rdf-schema#comment
"We conclude that API M358R inhibits FVIIa by forming inhibitory complexes of the serpin type more rapidly than AT in the absence of heparin."
xsd:string
http://purl.uniprot.org/uniprot/#_E8D95696EB4E5B87B100D560C90B5BF62D5980362D7F1F7E1B894248249F504E272197A132786424C3263C89B7E0E755
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2302BBE2C5FCD6A4A10FBA3543098D3C54BB2240D5C2464360344B3B3BE41FB2236FA3B474319D9988DC20411BD6A127
http://purl.uniprot.org/uniprot/Q9UHK1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2302BBE2C5FCD6A4A10FBA3543098D3C54BB2240D5C2464360344B3B3BE41FB2236FA3B474319D9988DC20411BD6A127
http://purl.uniprot.org/uniprot/#_Q9UHK1-mappedCitation-26797521
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2302BBE2C5FCD6A4A10FBA3543098D3C54BB2240D5C2464360344B3B3BE41FB2236FA3B474319D9988DC20411BD6A127