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DESCRIBE <http://purl.uniprot.org/SHA-384/72B7BB440A67E5B24058434EB57804DA01041B7806F6BE2C410676081F84B45C927E2D496D929741F1FBDEE2F5F5998B>
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http://purl.uniprot.org/SHA-384/72B7BB440A67E5B24058434EB57804DA01041B7806F6BE2C410676081F84B45C927E2D496D929741F1FBDEE2F5F5998B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/72B7BB440A67E5B24058434EB57804DA01041B7806F6BE2C410676081F84B45C927E2D496D929741F1FBDEE2F5F5998B
http://www.w3.org/2000/01/rdf-schema#comment
"In patients with MYH11 or ACTA2 variants the effect of intronic variants on splicing was demonstrated on the mRNA level in the induced smooth muscle cell (SMC) allowing classification into pathogenic or nonpathogenic variants."
xsd:string
http://purl.uniprot.org/uniprot/#_FFEAEAE4617447C6401E80AA97950642C1D1FA5845D67F40083EC230464619645FDC957A9270AAD580BA8CF0B83BF963
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/72B7BB440A67E5B24058434EB57804DA01041B7806F6BE2C410676081F84B45C927E2D496D929741F1FBDEE2F5F5998B
http://purl.uniprot.org/uniprot/P35749
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/72B7BB440A67E5B24058434EB57804DA01041B7806F6BE2C410676081F84B45C927E2D496D929741F1FBDEE2F5F5998B
http://purl.uniprot.org/uniprot/#_P35749-mappedCitation-28074631
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/72B7BB440A67E5B24058434EB57804DA01041B7806F6BE2C410676081F84B45C927E2D496D929741F1FBDEE2F5F5998B