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DESCRIBE <http://purl.uniprot.org/SHA-384/B6B6B0A327B499521E73D9319899B8593EF04A0B13C16DE9F06B8370A6B617C1FCBC84664A66D113F0E8AF1490016788>
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http://purl.uniprot.org/SHA-384/B6B6B0A327B499521E73D9319899B8593EF04A0B13C16DE9F06B8370A6B617C1FCBC84664A66D113F0E8AF1490016788
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B6B6B0A327B499521E73D9319899B8593EF04A0B13C16DE9F06B8370A6B617C1FCBC84664A66D113F0E8AF1490016788
http://www.w3.org/2000/01/rdf-schema#comment
"Data indicate that MEF2C missense de novo mutations in severe mental retardation showed diminished MECP2 and CDKL5 expression; Observational study of gene-disease association. (HuGE Navigator)"
xsd:string
http://purl.uniprot.org/uniprot/#_952B29F2CE748A507FE3390F0A4EF6AFEF81BB79C5C7C484DBC1828245323704EBA9889E0A686CB2879CB6B707A77996
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B6B6B0A327B499521E73D9319899B8593EF04A0B13C16DE9F06B8370A6B617C1FCBC84664A66D113F0E8AF1490016788
http://purl.uniprot.org/uniprot/A0A0D9SFD0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B6B6B0A327B499521E73D9319899B8593EF04A0B13C16DE9F06B8370A6B617C1FCBC84664A66D113F0E8AF1490016788
http://purl.uniprot.org/uniprot/#_A0A0D9SFD0-mappedCitation-20513142
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B6B6B0A327B499521E73D9319899B8593EF04A0B13C16DE9F06B8370A6B617C1FCBC84664A66D113F0E8AF1490016788