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DESCRIBE <http://purl.uniprot.org/SHA-384/E634510D344DB2E48677F4EB4B42776EE93E903377AB19B48A17A2AA500154155054C43BAC270E79869DA7FE5F020000>
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http://purl.uniprot.org/SHA-384/E634510D344DB2E48677F4EB4B42776EE93E903377AB19B48A17A2AA500154155054C43BAC270E79869DA7FE5F020000
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E634510D344DB2E48677F4EB4B42776EE93E903377AB19B48A17A2AA500154155054C43BAC270E79869DA7FE5F020000
http://www.w3.org/2000/01/rdf-schema#comment
"study 94.9% of the partial D samples revealed altered RHCE variant alleles and 5.7% of the samples with altered RHD allele predicted partial c partial e and the lack of the high prevalence hr(B) and hr(S) antigens."
xsd:string
http://purl.uniprot.org/uniprot/#_1BFF4CD5B2E8720FA01190FC2667FD2D584A35A2B86C322D1D68AF89F678C38620020E6052F122DA6AD8830F3D70645B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E634510D344DB2E48677F4EB4B42776EE93E903377AB19B48A17A2AA500154155054C43BAC270E79869DA7FE5F020000
http://purl.uniprot.org/uniprot/A0A089VLV6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E634510D344DB2E48677F4EB4B42776EE93E903377AB19B48A17A2AA500154155054C43BAC270E79869DA7FE5F020000
http://purl.uniprot.org/uniprot/#_A0A089VLV6-mappedCitation-27111588
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E634510D344DB2E48677F4EB4B42776EE93E903377AB19B48A17A2AA500154155054C43BAC270E79869DA7FE5F020000