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DESCRIBE <http://purl.uniprot.org/SHA-384/86F37DC027E15C47A001E689DB56B6FD1CAC2F648BCB3204CCC4BDA43D9F31BA941E0F0CDE202924B4FE7C4463BF2CDA>
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http://purl.uniprot.org/SHA-384/86F37DC027E15C47A001E689DB56B6FD1CAC2F648BCB3204CCC4BDA43D9F31BA941E0F0CDE202924B4FE7C4463BF2CDA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/86F37DC027E15C47A001E689DB56B6FD1CAC2F648BCB3204CCC4BDA43D9F31BA941E0F0CDE202924B4FE7C4463BF2CDA
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of genotype prevalence. (HuGE Navigator); Nine genetic variants were identified in the IMPDH2 gene with frequencies of the rarer alleles ranging from 0.5 to 10.2%."
xsd:string
http://purl.uniprot.org/uniprot/#_2BD227AD8CE14618B142460F17090C2CBDD3F5C78E4DB42542BC6D97C57E258971B1A9CD992320A100EEE7E2873F9DEC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/86F37DC027E15C47A001E689DB56B6FD1CAC2F648BCB3204CCC4BDA43D9F31BA941E0F0CDE202924B4FE7C4463BF2CDA
http://purl.uniprot.org/uniprot/A0A384N6C2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/86F37DC027E15C47A001E689DB56B6FD1CAC2F648BCB3204CCC4BDA43D9F31BA941E0F0CDE202924B4FE7C4463BF2CDA
http://purl.uniprot.org/uniprot/#_A0A384N6C2-mappedCitation-17496727
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/86F37DC027E15C47A001E689DB56B6FD1CAC2F648BCB3204CCC4BDA43D9F31BA941E0F0CDE202924B4FE7C4463BF2CDA