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DESCRIBE <http://purl.uniprot.org/SHA-384/B87CCE7BF6058A29F6A6303FD39866AB9E3EE072B311E62FFBEB770B2E4FA7716BE6AFA332F9736228E63CE5BF39C606>
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http://purl.uniprot.org/SHA-384/B87CCE7BF6058A29F6A6303FD39866AB9E3EE072B311E62FFBEB770B2E4FA7716BE6AFA332F9736228E63CE5BF39C606
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B87CCE7BF6058A29F6A6303FD39866AB9E3EE072B311E62FFBEB770B2E4FA7716BE6AFA332F9736228E63CE5BF39C606
http://www.w3.org/2000/01/rdf-schema#comment
"Screening of the exons in hypertrophic cardiomyopathy revealed two variations - one novel frame shift mutation in exon 19 at the nucleotide position 11577-11578 and one novel single nucleotide polymorphism (SNP) in codon 1093 of exon 31."
xsd:string
http://purl.uniprot.org/uniprot/#_02FF8FED55B91D11AB896771B9D79D0B98C38DED17FF4D6F56755798859DBDEFC2D3CC6B7134DCD40C271361945EFA12
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B87CCE7BF6058A29F6A6303FD39866AB9E3EE072B311E62FFBEB770B2E4FA7716BE6AFA332F9736228E63CE5BF39C606
http://purl.uniprot.org/uniprot/B6D426
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B87CCE7BF6058A29F6A6303FD39866AB9E3EE072B311E62FFBEB770B2E4FA7716BE6AFA332F9736228E63CE5BF39C606
http://purl.uniprot.org/uniprot/#_B6D426-mappedCitation-18273486
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B87CCE7BF6058A29F6A6303FD39866AB9E3EE072B311E62FFBEB770B2E4FA7716BE6AFA332F9736228E63CE5BF39C606