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DESCRIBE <http://purl.uniprot.org/SHA-384/E2C1AB98672EC7D5F9095F1EAEA159CFF7F4CB3FF84B02064F0BE7C75407CBA098A8EEF7960D19760AB07F8E0EA0DE32>
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http://purl.uniprot.org/SHA-384/E2C1AB98672EC7D5F9095F1EAEA159CFF7F4CB3FF84B02064F0BE7C75407CBA098A8EEF7960D19760AB07F8E0EA0DE32
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E2C1AB98672EC7D5F9095F1EAEA159CFF7F4CB3FF84B02064F0BE7C75407CBA098A8EEF7960D19760AB07F8E0EA0DE32
http://www.w3.org/2000/01/rdf-schema#comment
"Perrault syndrome and DBP deficiency overlap clinically and Perrault syndrome is genetically heterogeneous."
xsd:string
http://purl.uniprot.org/uniprot/#_B3ACFF27A314FCF18F8D12F63A2B89956FE13986ECCEFBE7F5307BC26EAA555692FAD4E1E1C907363BA5C26A5E22FDCB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E2C1AB98672EC7D5F9095F1EAEA159CFF7F4CB3FF84B02064F0BE7C75407CBA098A8EEF7960D19760AB07F8E0EA0DE32
http://purl.uniprot.org/uniprot/B2R659
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E2C1AB98672EC7D5F9095F1EAEA159CFF7F4CB3FF84B02064F0BE7C75407CBA098A8EEF7960D19760AB07F8E0EA0DE32
http://purl.uniprot.org/uniprot/#_B2R659-mappedCitation-20673864
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E2C1AB98672EC7D5F9095F1EAEA159CFF7F4CB3FF84B02064F0BE7C75407CBA098A8EEF7960D19760AB07F8E0EA0DE32