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DESCRIBE <http://purl.uniprot.org/SHA-384/64B56EEF0A3D7BCA1B07124194B3ACA49C03B7F97F057F641E3CE49534E95CAE8A779F7538B4C0F350EB8E64A00DB659>
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http://purl.uniprot.org/SHA-384/64B56EEF0A3D7BCA1B07124194B3ACA49C03B7F97F057F641E3CE49534E95CAE8A779F7538B4C0F350EB8E64A00DB659
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/64B56EEF0A3D7BCA1B07124194B3ACA49C03B7F97F057F641E3CE49534E95CAE8A779F7538B4C0F350EB8E64A00DB659
http://www.w3.org/2000/01/rdf-schema#comment
"Our study indicates that different mutations in the RDH5 gene can cause phenotypic variations of either fundus albipunctatus or familial fleck retina with night blindness."
xsd:string
http://purl.uniprot.org/uniprot/#_8CA02F51FD32A8CCC8DDED7544AE6DC8F01151703874308FE7CBDF81BD6DCDEFE400A0029AD34269BE64C09A2C847CA5
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/64B56EEF0A3D7BCA1B07124194B3ACA49C03B7F97F057F641E3CE49534E95CAE8A779F7538B4C0F350EB8E64A00DB659
http://purl.uniprot.org/uniprot/Q92781
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/64B56EEF0A3D7BCA1B07124194B3ACA49C03B7F97F057F641E3CE49534E95CAE8A779F7538B4C0F350EB8E64A00DB659
http://purl.uniprot.org/uniprot/#_Q92781-mappedCitation-16637847
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/64B56EEF0A3D7BCA1B07124194B3ACA49C03B7F97F057F641E3CE49534E95CAE8A779F7538B4C0F350EB8E64A00DB659