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DESCRIBE <http://purl.uniprot.org/SHA-384/1982F33A9F0B0F23A082F75A6162CACCE8FB7A0B7752A3244087B0B1AF13E90030492F6DDB6859BCBD8BC791A8C28EAC>
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http://purl.uniprot.org/SHA-384/1982F33A9F0B0F23A082F75A6162CACCE8FB7A0B7752A3244087B0B1AF13E90030492F6DDB6859BCBD8BC791A8C28EAC
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1982F33A9F0B0F23A082F75A6162CACCE8FB7A0B7752A3244087B0B1AF13E90030492F6DDB6859BCBD8BC791A8C28EAC
http://www.w3.org/2000/01/rdf-schema#comment
"The findings from these cases further expand the clinical spectrum associated with mutations in the LMNA gene."
xsd:string
http://purl.uniprot.org/uniprot/#_B70663F680CFE84A7DBD75579E4AEED6FFDCD2A18A96BE456CEAB8C5CA2BDA7D0362931B7502541803403E5AD372FD2B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1982F33A9F0B0F23A082F75A6162CACCE8FB7A0B7752A3244087B0B1AF13E90030492F6DDB6859BCBD8BC791A8C28EAC
http://purl.uniprot.org/uniprot/A0A384MQX1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1982F33A9F0B0F23A082F75A6162CACCE8FB7A0B7752A3244087B0B1AF13E90030492F6DDB6859BCBD8BC791A8C28EAC
http://purl.uniprot.org/uniprot/#_A0A384MQX1-mappedCitation-17701980
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1982F33A9F0B0F23A082F75A6162CACCE8FB7A0B7752A3244087B0B1AF13E90030492F6DDB6859BCBD8BC791A8C28EAC