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DESCRIBE <http://purl.uniprot.org/SHA-384/39A1CEF86E7441E5B82F8B7357EF677A02DF2FE6AAABE7B7F6DCF6F2EFCBEED33B0406175C54E961F3F36D532F41B960>
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http://purl.uniprot.org/SHA-384/39A1CEF86E7441E5B82F8B7357EF677A02DF2FE6AAABE7B7F6DCF6F2EFCBEED33B0406175C54E961F3F36D532F41B960
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/39A1CEF86E7441E5B82F8B7357EF677A02DF2FE6AAABE7B7F6DCF6F2EFCBEED33B0406175C54E961F3F36D532F41B960
http://www.w3.org/2000/01/rdf-schema#comment
"The study documents that among the HbE beta thalassemia patients with varying severity an exon mutation in AHSP is significantly prevalent only among the transfusion-dependent beta-thalassemia patients."
xsd:string
http://purl.uniprot.org/uniprot/#_7A05E4B3E9EDBC2E3A4B24C22D62DC16DBEA0DC92F7CB9DEAF5DEF2AAE346ED92B23AF825CC1621F2696C13F526B8BE0
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/39A1CEF86E7441E5B82F8B7357EF677A02DF2FE6AAABE7B7F6DCF6F2EFCBEED33B0406175C54E961F3F36D532F41B960
http://purl.uniprot.org/uniprot/Q549J4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/39A1CEF86E7441E5B82F8B7357EF677A02DF2FE6AAABE7B7F6DCF6F2EFCBEED33B0406175C54E961F3F36D532F41B960
http://purl.uniprot.org/uniprot/#_Q549J4-mappedCitation-31190133
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/39A1CEF86E7441E5B82F8B7357EF677A02DF2FE6AAABE7B7F6DCF6F2EFCBEED33B0406175C54E961F3F36D532F41B960