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DESCRIBE <http://purl.uniprot.org/SHA-384/6F33E3F4EC83B5F3105FB4BD9AA0A91FDE85CF44B7E292450C057C4155C9D8F990B5C11873D3272C900653F7772D19E8>
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http://purl.uniprot.org/SHA-384/6F33E3F4EC83B5F3105FB4BD9AA0A91FDE85CF44B7E292450C057C4155C9D8F990B5C11873D3272C900653F7772D19E8
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6F33E3F4EC83B5F3105FB4BD9AA0A91FDE85CF44B7E292450C057C4155C9D8F990B5C11873D3272C900653F7772D19E8
http://www.w3.org/2000/01/rdf-schema#comment
"The study's results confirmed that MYH11 is a candidate gene for Megacystis-microcolon-intestinal-hypoperistalsis syndrome with autosomal recessive (AR) inheritance and expanded the mutation spectrum for this clinical condition."
xsd:string
http://purl.uniprot.org/uniprot/#_753D1D92728AC40763787D170AD2C9A174066CDD7DA0A89E4D5003BD3886D5C771AE23F3B885B655F1248B853E96260E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6F33E3F4EC83B5F3105FB4BD9AA0A91FDE85CF44B7E292450C057C4155C9D8F990B5C11873D3272C900653F7772D19E8
http://purl.uniprot.org/uniprot/Q66K75
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6F33E3F4EC83B5F3105FB4BD9AA0A91FDE85CF44B7E292450C057C4155C9D8F990B5C11873D3272C900653F7772D19E8
http://purl.uniprot.org/uniprot/#_Q66K75-mappedCitation-31427716
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6F33E3F4EC83B5F3105FB4BD9AA0A91FDE85CF44B7E292450C057C4155C9D8F990B5C11873D3272C900653F7772D19E8