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DESCRIBE <http://purl.uniprot.org/SHA-384/4E76FA63BE9A4744743B1870810094EEEBCFF3BF663A0E95F71DA7E5AD7D254EBCE979F60D3DBF6CB2EAD1C51A83C522>
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http://purl.uniprot.org/SHA-384/4E76FA63BE9A4744743B1870810094EEEBCFF3BF663A0E95F71DA7E5AD7D254EBCE979F60D3DBF6CB2EAD1C51A83C522
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4E76FA63BE9A4744743B1870810094EEEBCFF3BF663A0E95F71DA7E5AD7D254EBCE979F60D3DBF6CB2EAD1C51A83C522
http://www.w3.org/2000/01/rdf-schema#comment
"Genotype-phenotype correlation between CNL5 gene mutations and CNL5 disease symptoms."
xsd:string
http://purl.uniprot.org/uniprot/#_C46819244E74CCED63DA4E98CA48AE5042389EFE6C893DCD71C0931E8C7E3F2BA749F43B4AEA62C526BD135EB8215596
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4E76FA63BE9A4744743B1870810094EEEBCFF3BF663A0E95F71DA7E5AD7D254EBCE979F60D3DBF6CB2EAD1C51A83C522
http://purl.uniprot.org/uniprot/O75503
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4E76FA63BE9A4744743B1870810094EEEBCFF3BF663A0E95F71DA7E5AD7D254EBCE979F60D3DBF6CB2EAD1C51A83C522
http://purl.uniprot.org/uniprot/#_O75503-mappedCitation-28542837
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4E76FA63BE9A4744743B1870810094EEEBCFF3BF663A0E95F71DA7E5AD7D254EBCE979F60D3DBF6CB2EAD1C51A83C522