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DESCRIBE <http://purl.uniprot.org/SHA-384/5C6B107ADE0BB65B0533285AD59DD4DE76AEBD17B2B30A8D9BA266C556C3B90D9172616BE6F6CF9D7549D4C887AA70A0>
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http://purl.uniprot.org/SHA-384/5C6B107ADE0BB65B0533285AD59DD4DE76AEBD17B2B30A8D9BA266C556C3B90D9172616BE6F6CF9D7549D4C887AA70A0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5C6B107ADE0BB65B0533285AD59DD4DE76AEBD17B2B30A8D9BA266C556C3B90D9172616BE6F6CF9D7549D4C887AA70A0
http://www.w3.org/2000/01/rdf-schema#comment
"Our results expand the frequency and spectrum of mutations at RPGR and RP2 as well as their associated clinical phenotypes in Chinese patients."
xsd:string
http://purl.uniprot.org/uniprot/#_560CACD276970E59111B2C8D84783D1E37123147A582F5E51F44A8509EA53DE5C3FAE1E80CAF72497C11D72F51DC1589
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5C6B107ADE0BB65B0533285AD59DD4DE76AEBD17B2B30A8D9BA266C556C3B90D9172616BE6F6CF9D7549D4C887AA70A0
http://purl.uniprot.org/uniprot/A0A1B2JLU2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5C6B107ADE0BB65B0533285AD59DD4DE76AEBD17B2B30A8D9BA266C556C3B90D9172616BE6F6CF9D7549D4C887AA70A0
http://purl.uniprot.org/uniprot/#_A0A1B2JLU2-mappedCitation-20021257
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5C6B107ADE0BB65B0533285AD59DD4DE76AEBD17B2B30A8D9BA266C556C3B90D9172616BE6F6CF9D7549D4C887AA70A0