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DESCRIBE <http://purl.uniprot.org/SHA-384/9EB6EF2AC8EBCD45A178AA660CB2A98E0290DA7F8BF358007E5070D9C08E7DE2AF4230716EBC07BF98AAC2D20D1CAA57>
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http://purl.uniprot.org/SHA-384/9EB6EF2AC8EBCD45A178AA660CB2A98E0290DA7F8BF358007E5070D9C08E7DE2AF4230716EBC07BF98AAC2D20D1CAA57
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9EB6EF2AC8EBCD45A178AA660CB2A98E0290DA7F8BF358007E5070D9C08E7DE2AF4230716EBC07BF98AAC2D20D1CAA57
http://www.w3.org/2000/01/rdf-schema#comment
"coexpression of the G6PD African A- mutation with UGT1A1 and/or SLCO1B1 variants was seen more frequently in neonatal hyperbilirubinemia; Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)"
xsd:string
http://purl.uniprot.org/uniprot/#_DBCBFAD4581F626653F40CA1F06CAEEA588C769FC699E681A34693A70BD602B66E8F18C7C6AFEDB7247254E2B7FB0D21
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9EB6EF2AC8EBCD45A178AA660CB2A98E0290DA7F8BF358007E5070D9C08E7DE2AF4230716EBC07BF98AAC2D20D1CAA57
http://purl.uniprot.org/uniprot/B4DYA7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9EB6EF2AC8EBCD45A178AA660CB2A98E0290DA7F8BF358007E5070D9C08E7DE2AF4230716EBC07BF98AAC2D20D1CAA57
http://purl.uniprot.org/uniprot/#_B4DYA7-mappedCitation-19858149
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9EB6EF2AC8EBCD45A178AA660CB2A98E0290DA7F8BF358007E5070D9C08E7DE2AF4230716EBC07BF98AAC2D20D1CAA57