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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/7E36CADF9DA649B9631CDDF0F05896674037217A633579A00F8C94F8F420F20CD8F8076EA9D72DB3E779F54F3B977B89>
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http://purl.uniprot.org/SHA-384/7E36CADF9DA649B9631CDDF0F05896674037217A633579A00F8C94F8F420F20CD8F8076EA9D72DB3E779F54F3B977B89
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7E36CADF9DA649B9631CDDF0F05896674037217A633579A00F8C94F8F420F20CD8F8076EA9D72DB3E779F54F3B977B89
http://www.w3.org/2000/01/rdf-schema#comment
"Heterozygous mutations of the LMNA gene were found in two patients with coronary artery disease with a Werner syndrome-like form of progeria."
xsd:string
http://purl.uniprot.org/uniprot/#_F12F82C2BC2492B3C9CFDCD79D8D201443DB37D2B9B4A26A858BF1102DEB3351D9C166D7270BCB2EB6C7411E14BDDD64
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7E36CADF9DA649B9631CDDF0F05896674037217A633579A00F8C94F8F420F20CD8F8076EA9D72DB3E779F54F3B977B89
http://purl.uniprot.org/uniprot/Q5TCI8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7E36CADF9DA649B9631CDDF0F05896674037217A633579A00F8C94F8F420F20CD8F8076EA9D72DB3E779F54F3B977B89
http://purl.uniprot.org/uniprot/#_Q5TCI8-mappedCitation-22065502
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7E36CADF9DA649B9631CDDF0F05896674037217A633579A00F8C94F8F420F20CD8F8076EA9D72DB3E779F54F3B977B89