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DESCRIBE <http://purl.uniprot.org/SHA-384/16CCF4DE4C206B04BD00E36914E647CF842C61D20F0C69A97F2B6EDCA987F8E9B3F09D07E7588CA7792F3B454888E08D>
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http://purl.uniprot.org/SHA-384/16CCF4DE4C206B04BD00E36914E647CF842C61D20F0C69A97F2B6EDCA987F8E9B3F09D07E7588CA7792F3B454888E08D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/16CCF4DE4C206B04BD00E36914E647CF842C61D20F0C69A97F2B6EDCA987F8E9B3F09D07E7588CA7792F3B454888E08D
http://www.w3.org/2000/01/rdf-schema#comment
"Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants."
xsd:string
http://purl.uniprot.org/uniprot/#_54A57C2FF8D538D02DC7E77C8880E6A3F9B446DD491E65E355FF763E8075DA2581CF283713B553AE5A36BE3FE9C6AC1B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/16CCF4DE4C206B04BD00E36914E647CF842C61D20F0C69A97F2B6EDCA987F8E9B3F09D07E7588CA7792F3B454888E08D
http://purl.uniprot.org/uniprot/A0A286YFI8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/16CCF4DE4C206B04BD00E36914E647CF842C61D20F0C69A97F2B6EDCA987F8E9B3F09D07E7588CA7792F3B454888E08D
http://purl.uniprot.org/uniprot/#_A0A286YFI8-mappedCitation-35457110
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/16CCF4DE4C206B04BD00E36914E647CF842C61D20F0C69A97F2B6EDCA987F8E9B3F09D07E7588CA7792F3B454888E08D