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DESCRIBE <http://purl.uniprot.org/SHA-384/F2D9C56E42DF24E5387FF69A37E6766F3446DC8FEC4C0BB2AD90FDCE8D8BDE3FEABF6AE20BB7CDFC769DB06A83DAFC20>
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http://purl.uniprot.org/SHA-384/F2D9C56E42DF24E5387FF69A37E6766F3446DC8FEC4C0BB2AD90FDCE8D8BDE3FEABF6AE20BB7CDFC769DB06A83DAFC20
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F2D9C56E42DF24E5387FF69A37E6766F3446DC8FEC4C0BB2AD90FDCE8D8BDE3FEABF6AE20BB7CDFC769DB06A83DAFC20
http://www.w3.org/2000/01/rdf-schema#comment
"This is the first report of a patient with hereditary angioedema due to a homozygous de novo null mutation of the C1NH gene."
xsd:string
http://purl.uniprot.org/uniprot/#_F614EA5A78AC57F89A3E406E64EEE58596B5E442EFDFFEDB0DEAF1447416D85D506A7862F44D8E62E1651BB2451E87C3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F2D9C56E42DF24E5387FF69A37E6766F3446DC8FEC4C0BB2AD90FDCE8D8BDE3FEABF6AE20BB7CDFC769DB06A83DAFC20
http://purl.uniprot.org/uniprot/E9PK97
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F2D9C56E42DF24E5387FF69A37E6766F3446DC8FEC4C0BB2AD90FDCE8D8BDE3FEABF6AE20BB7CDFC769DB06A83DAFC20
http://purl.uniprot.org/uniprot/#_E9PK97-mappedCitation-23688413
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F2D9C56E42DF24E5387FF69A37E6766F3446DC8FEC4C0BB2AD90FDCE8D8BDE3FEABF6AE20BB7CDFC769DB06A83DAFC20