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DESCRIBE <http://purl.uniprot.org/SHA-384/9DDC2A11E692BFA0E14658D600A2E1D566884DAAF117828956A0E36E54F930C421BFB00BF2FC3566A1810AEE6134315D>
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http://purl.uniprot.org/SHA-384/9DDC2A11E692BFA0E14658D600A2E1D566884DAAF117828956A0E36E54F930C421BFB00BF2FC3566A1810AEE6134315D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9DDC2A11E692BFA0E14658D600A2E1D566884DAAF117828956A0E36E54F930C421BFB00BF2FC3566A1810AEE6134315D
http://www.w3.org/2000/01/rdf-schema#comment
"All family members with maculopathy consistent with Best disease (n = 10) had an amino acid-changing mutation in the VMD2 gene."
xsd:string
http://purl.uniprot.org/uniprot/#_F82A7AAAABB0DEA04AE64F3EAD9DF1E7BBED99D7F947A74F3F737828B92A09DF07CAB9E707BE0E843F459F1AB4EAD00F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9DDC2A11E692BFA0E14658D600A2E1D566884DAAF117828956A0E36E54F930C421BFB00BF2FC3566A1810AEE6134315D
http://purl.uniprot.org/uniprot/A0A0S2Z579
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9DDC2A11E692BFA0E14658D600A2E1D566884DAAF117828956A0E36E54F930C421BFB00BF2FC3566A1810AEE6134315D
http://purl.uniprot.org/uniprot/#_A0A0S2Z579-mappedCitation-13129869
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9DDC2A11E692BFA0E14658D600A2E1D566884DAAF117828956A0E36E54F930C421BFB00BF2FC3566A1810AEE6134315D