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DESCRIBE <http://purl.uniprot.org/SHA-384/26037E4883407F78B456B7461900D912DA9257680DA9351986D89BD93DFCA3FB0344028970EE52CE14E55B6604FB6225>
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http://purl.uniprot.org/SHA-384/26037E4883407F78B456B7461900D912DA9257680DA9351986D89BD93DFCA3FB0344028970EE52CE14E55B6604FB6225
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/26037E4883407F78B456B7461900D912DA9257680DA9351986D89BD93DFCA3FB0344028970EE52CE14E55B6604FB6225
http://www.w3.org/2000/01/rdf-schema#comment
"the FRIZZLED2 mutation is a de novo novel cause for autosomal dominant omodysplasia."
xsd:string
http://purl.uniprot.org/uniprot/#_A41E085E7711C668A6102A7D1299BCC4BF063CCDF45FC0D5D41F2771057ACC052198BB5521FBA2410B3DB24BE2C89F9A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/26037E4883407F78B456B7461900D912DA9257680DA9351986D89BD93DFCA3FB0344028970EE52CE14E55B6604FB6225
http://purl.uniprot.org/uniprot/Q86UZ8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/26037E4883407F78B456B7461900D912DA9257680DA9351986D89BD93DFCA3FB0344028970EE52CE14E55B6604FB6225
http://purl.uniprot.org/uniprot/#_Q86UZ8-mappedCitation-25759469
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/26037E4883407F78B456B7461900D912DA9257680DA9351986D89BD93DFCA3FB0344028970EE52CE14E55B6604FB6225