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DESCRIBE <http://purl.uniprot.org/SHA-384/B821C673761B3A323B0FA401D4D82A75DFEFAFFFEFA92B4C6F50BBAB21DB76AC4A234FA080E5F210057733392205F0DC>
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http://purl.uniprot.org/SHA-384/B821C673761B3A323B0FA401D4D82A75DFEFAFFFEFA92B4C6F50BBAB21DB76AC4A234FA080E5F210057733392205F0DC
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B821C673761B3A323B0FA401D4D82A75DFEFAFFFEFA92B4C6F50BBAB21DB76AC4A234FA080E5F210057733392205F0DC
http://www.w3.org/2000/01/rdf-schema#comment
"Patients from a family with ectopia lentis et pupillae (ELP) in four generations have autosomal recessive ELP caused by novel mutations in ADAMTSL4."
xsd:string
http://purl.uniprot.org/uniprot/#_853032152DA355D921C631658F723A57D4417DD59822E92C3C26DD3CAE257BD9863017950FFD1A3E929EF4620BF001A3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B821C673761B3A323B0FA401D4D82A75DFEFAFFFEFA92B4C6F50BBAB21DB76AC4A234FA080E5F210057733392205F0DC
http://purl.uniprot.org/uniprot/Q9UFG7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B821C673761B3A323B0FA401D4D82A75DFEFAFFFEFA92B4C6F50BBAB21DB76AC4A234FA080E5F210057733392205F0DC
http://purl.uniprot.org/uniprot/#_Q9UFG7-mappedCitation-23426735
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B821C673761B3A323B0FA401D4D82A75DFEFAFFFEFA92B4C6F50BBAB21DB76AC4A234FA080E5F210057733392205F0DC