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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/A2E9A3C7B0FA95A0B9014BF8E756A54843A28F208B1708A7297E06EC5AFB1CA157157E99F48590A4223F18205EF29C4E>
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http://purl.uniprot.org/SHA-384/A2E9A3C7B0FA95A0B9014BF8E756A54843A28F208B1708A7297E06EC5AFB1CA157157E99F48590A4223F18205EF29C4E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A2E9A3C7B0FA95A0B9014BF8E756A54843A28F208B1708A7297E06EC5AFB1CA157157E99F48590A4223F18205EF29C4E
http://www.w3.org/2000/01/rdf-schema#comment
"our results provide evidence that mutations in A2ML1 are a cause of Noonan-like syndrome with a variable phenotype ranging from severe to very mild."
xsd:string
http://purl.uniprot.org/uniprot/#_716BB423050DC3500DD3D3D897A85345A6FAB61BE682B36E41501ADD825DEFD1E8B87302FF790612ACB9B4C78B457DC0
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A2E9A3C7B0FA95A0B9014BF8E756A54843A28F208B1708A7297E06EC5AFB1CA157157E99F48590A4223F18205EF29C4E
http://purl.uniprot.org/uniprot/A8K2U0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A2E9A3C7B0FA95A0B9014BF8E756A54843A28F208B1708A7297E06EC5AFB1CA157157E99F48590A4223F18205EF29C4E
http://purl.uniprot.org/uniprot/#_A8K2U0-mappedCitation-24939586
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A2E9A3C7B0FA95A0B9014BF8E756A54843A28F208B1708A7297E06EC5AFB1CA157157E99F48590A4223F18205EF29C4E