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DESCRIBE <http://purl.uniprot.org/SHA-384/4AC8E4349D273B050228D0E5C8F50F00ADD8516C3CE3AC33CEB7B0DC74AC2230D1081B5B698A164D980ED07035D83C86>
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http://purl.uniprot.org/SHA-384/4AC8E4349D273B050228D0E5C8F50F00ADD8516C3CE3AC33CEB7B0DC74AC2230D1081B5B698A164D980ED07035D83C86
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4AC8E4349D273B050228D0E5C8F50F00ADD8516C3CE3AC33CEB7B0DC74AC2230D1081B5B698A164D980ED07035D83C86
http://www.w3.org/2000/01/rdf-schema#comment
"Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy."
xsd:string
http://purl.uniprot.org/uniprot/#_C9FE0D468F0E3E6FA20938B8EDF776DD7ED5C51999AEEE7C7058C4D46140A49FAAD28A417D5E5E97628BB733656C9847
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4AC8E4349D273B050228D0E5C8F50F00ADD8516C3CE3AC33CEB7B0DC74AC2230D1081B5B698A164D980ED07035D83C86
http://purl.uniprot.org/uniprot/R9UMG9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4AC8E4349D273B050228D0E5C8F50F00ADD8516C3CE3AC33CEB7B0DC74AC2230D1081B5B698A164D980ED07035D83C86
http://purl.uniprot.org/uniprot/#_R9UMG9-mappedCitation-36115991
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4AC8E4349D273B050228D0E5C8F50F00ADD8516C3CE3AC33CEB7B0DC74AC2230D1081B5B698A164D980ED07035D83C86