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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/E17252A76F412DC63EF341F53B9F82C54BE368A061658824D660F231C900C42A82280CBE74B9EDC236B7DD23E0F9ACB0>
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http://purl.uniprot.org/SHA-384/E17252A76F412DC63EF341F53B9F82C54BE368A061658824D660F231C900C42A82280CBE74B9EDC236B7DD23E0F9ACB0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E17252A76F412DC63EF341F53B9F82C54BE368A061658824D660F231C900C42A82280CBE74B9EDC236B7DD23E0F9ACB0
http://www.w3.org/2000/01/rdf-schema#comment
"results showed high prevalence of AAT deficiency allele in the Saudi population; of 158 subjects 11.39% were carriers for S mutation 2.53% were carriers for Z mutation; SZ genotype was present in 3.8%; SS genotype was present in 1.9%"
xsd:string
http://purl.uniprot.org/uniprot/#_EE1A0DB5E8422589F5DFC73AFA2EF2DDCBCF4C2C14EBF1CBE18CB7F167672CD0BAECA7E769B1DC4F009E1A4E116773F6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E17252A76F412DC63EF341F53B9F82C54BE368A061658824D660F231C900C42A82280CBE74B9EDC236B7DD23E0F9ACB0
http://purl.uniprot.org/uniprot/A6YP93
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E17252A76F412DC63EF341F53B9F82C54BE368A061658824D660F231C900C42A82280CBE74B9EDC236B7DD23E0F9ACB0
http://purl.uniprot.org/uniprot/#_A6YP93-mappedCitation-21727732
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E17252A76F412DC63EF341F53B9F82C54BE368A061658824D660F231C900C42A82280CBE74B9EDC236B7DD23E0F9ACB0