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DESCRIBE <http://purl.uniprot.org/SHA-384/88324B6960ACA2D48C4C7600535AF9D5B592F9D11D68DA3D8E6F39695780538A233319BAC97BCD14263E14155EA81DCE>
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http://purl.uniprot.org/SHA-384/88324B6960ACA2D48C4C7600535AF9D5B592F9D11D68DA3D8E6F39695780538A233319BAC97BCD14263E14155EA81DCE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/88324B6960ACA2D48C4C7600535AF9D5B592F9D11D68DA3D8E6F39695780538A233319BAC97BCD14263E14155EA81DCE
http://www.w3.org/2000/01/rdf-schema#comment
"We report an unusual phenotype in a child with a clinical diagnosis of recessive Stargardt disease (STGD1) and two pathogenic variants in the ABCA4 gene."
xsd:string
http://purl.uniprot.org/uniprot/#_1897B081335DFA4E11BFB288367D04DDD203B5C8D8F0CD29C0315F9254AB6F96C1CCC906D373F9DB1E52C8296C898957
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/88324B6960ACA2D48C4C7600535AF9D5B592F9D11D68DA3D8E6F39695780538A233319BAC97BCD14263E14155EA81DCE
http://purl.uniprot.org/uniprot/B4DIX3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/88324B6960ACA2D48C4C7600535AF9D5B592F9D11D68DA3D8E6F39695780538A233319BAC97BCD14263E14155EA81DCE
http://purl.uniprot.org/uniprot/#_B4DIX3-mappedCitation-28726568
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/88324B6960ACA2D48C4C7600535AF9D5B592F9D11D68DA3D8E6F39695780538A233319BAC97BCD14263E14155EA81DCE