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DESCRIBE <http://purl.uniprot.org/SHA-384/C31894F609462E8775F8584FC77E21A3A46B2284C5AAD0EB1FD52D559CF8A1E30C94EC2406B781064F49480AC04A72AD>
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http://purl.uniprot.org/SHA-384/C31894F609462E8775F8584FC77E21A3A46B2284C5AAD0EB1FD52D559CF8A1E30C94EC2406B781064F49480AC04A72AD
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C31894F609462E8775F8584FC77E21A3A46B2284C5AAD0EB1FD52D559CF8A1E30C94EC2406B781064F49480AC04A72AD
http://www.w3.org/2000/01/rdf-schema#comment
"The missense mutation E82K in LMNA gene was associated with a malignant phenotype of severe clinical symptoms of familial dilated cardiomyopathy."
xsd:string
http://purl.uniprot.org/uniprot/#_04AF34596852EF2195A3D9EBDF4CE228FBC35FD62CAD5205678FA9EEA3EC61068C80B8090734DD6DC3C49E1AADBB1D85
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C31894F609462E8775F8584FC77E21A3A46B2284C5AAD0EB1FD52D559CF8A1E30C94EC2406B781064F49480AC04A72AD
http://purl.uniprot.org/uniprot/Q5TCI8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C31894F609462E8775F8584FC77E21A3A46B2284C5AAD0EB1FD52D559CF8A1E30C94EC2406B781064F49480AC04A72AD
http://purl.uniprot.org/uniprot/#_Q5TCI8-mappedCitation-16266469
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C31894F609462E8775F8584FC77E21A3A46B2284C5AAD0EB1FD52D559CF8A1E30C94EC2406B781064F49480AC04A72AD