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DESCRIBE <http://purl.uniprot.org/SHA-384/5E57285F46889C6CC3FEFCB3A5B027B16CF323039543FF8AD35CE5367059B133C15B62E28FBD2A4A905D6EB40053B013>
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http://purl.uniprot.org/SHA-384/5E57285F46889C6CC3FEFCB3A5B027B16CF323039543FF8AD35CE5367059B133C15B62E28FBD2A4A905D6EB40053B013
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5E57285F46889C6CC3FEFCB3A5B027B16CF323039543FF8AD35CE5367059B133C15B62E28FBD2A4A905D6EB40053B013
http://www.w3.org/2000/01/rdf-schema#comment
"Heterozygotes with hypermethylation of specific CpG sites in the G6PD promoter and preferential X-inactivation of the wild-type allele were at risk of enzyme deficiency."
xsd:string
http://purl.uniprot.org/uniprot/#_C3B017E98323A0FF2F1C1A2B1AD38E3C56F262451A6752F7CDC44B7381B334BD7D91DF3F65F72F0D6EB02F2D2D9A7089
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5E57285F46889C6CC3FEFCB3A5B027B16CF323039543FF8AD35CE5367059B133C15B62E28FBD2A4A905D6EB40053B013
http://purl.uniprot.org/uniprot/A0A2H4QGB2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5E57285F46889C6CC3FEFCB3A5B027B16CF323039543FF8AD35CE5367059B133C15B62E28FBD2A4A905D6EB40053B013
http://purl.uniprot.org/uniprot/#_A0A2H4QGB2-mappedCitation-24958328
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5E57285F46889C6CC3FEFCB3A5B027B16CF323039543FF8AD35CE5367059B133C15B62E28FBD2A4A905D6EB40053B013