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DESCRIBE <http://purl.uniprot.org/SHA-384/07AAF4C006794350C62CECC0EF3A65DBD154E9F8BBAFCC729484FFEC27C23F96EC0287224434C607E81B5802679A27FA>
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http://purl.uniprot.org/SHA-384/07AAF4C006794350C62CECC0EF3A65DBD154E9F8BBAFCC729484FFEC27C23F96EC0287224434C607E81B5802679A27FA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/07AAF4C006794350C62CECC0EF3A65DBD154E9F8BBAFCC729484FFEC27C23F96EC0287224434C607E81B5802679A27FA
http://www.w3.org/2000/01/rdf-schema#comment
"Detection of a novol homozygous GT transition in the first base of intron 11 (c.1428 1G>T) of the human serum albumin gene in two children with analbuminemia."
xsd:string
http://purl.uniprot.org/uniprot/#_F7A52E393F8906B84C789FAA4CF8C6E187E71076CA2907EB3DA9BB07FF02D83BF672DFC0F10BE7D2239A3D79DCA27D25
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/07AAF4C006794350C62CECC0EF3A65DBD154E9F8BBAFCC729484FFEC27C23F96EC0287224434C607E81B5802679A27FA
http://purl.uniprot.org/uniprot/P02768
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/07AAF4C006794350C62CECC0EF3A65DBD154E9F8BBAFCC729484FFEC27C23F96EC0287224434C607E81B5802679A27FA
http://purl.uniprot.org/uniprot/#_P02768-mappedCitation-22613267
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/07AAF4C006794350C62CECC0EF3A65DBD154E9F8BBAFCC729484FFEC27C23F96EC0287224434C607E81B5802679A27FA