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DESCRIBE <http://purl.uniprot.org/SHA-384/B869AB1F9D92A9FFA6048E0E215AF7F3915254B0E78ABC4DB9EE8FD365ED0B5259ADDB48486C1485E55B80A8FDFFBC5C>
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http://purl.uniprot.org/SHA-384/B869AB1F9D92A9FFA6048E0E215AF7F3915254B0E78ABC4DB9EE8FD365ED0B5259ADDB48486C1485E55B80A8FDFFBC5C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B869AB1F9D92A9FFA6048E0E215AF7F3915254B0E78ABC4DB9EE8FD365ED0B5259ADDB48486C1485E55B80A8FDFFBC5C
http://www.w3.org/2000/01/rdf-schema#comment
"the present results do not indicate that mutations in ACTG1 are a frequent cause of autosomal-dominant postlingual sensorineural hearing impairment in Norway nor Denmark."
xsd:string
http://purl.uniprot.org/uniprot/#_373D9265BBE6671421D348A6A04730C27115F2848899402CDE1489809448700591B2E3A9D900F00220A4586F82FD76D7
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B869AB1F9D92A9FFA6048E0E215AF7F3915254B0E78ABC4DB9EE8FD365ED0B5259ADDB48486C1485E55B80A8FDFFBC5C
http://purl.uniprot.org/uniprot/V9HVZ7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B869AB1F9D92A9FFA6048E0E215AF7F3915254B0E78ABC4DB9EE8FD365ED0B5259ADDB48486C1485E55B80A8FDFFBC5C
http://purl.uniprot.org/uniprot/#_V9HVZ7-mappedCitation-16773128
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B869AB1F9D92A9FFA6048E0E215AF7F3915254B0E78ABC4DB9EE8FD365ED0B5259ADDB48486C1485E55B80A8FDFFBC5C