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http://purl.uniprot.org/SHA-384/CD0D48C9F484A66FA4E438CF1EB50B9A8CBAD2E47F08F2A03400AA8614FC832A52F8BC5F3B9B075AD403A23B642A81DAhttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CD0D48C9F484A66FA4E438CF1EB50B9A8CBAD2E47F08F2A03400AA8614FC832A52F8BC5F3B9B075AD403A23B642A81DAhttp://www.w3.org/2000/01/rdf-schema#comment"To further understand FOXE3 involvement in this wide spectrum of ocular anomalies with 2 different patterns of inheritance we reviewed all individuals with ocular abnormalities described in the literature for which a FOXE3 mutation was identified. This review demonstrates that correlations exist between the mutation type mode of inheritance and the phenotype severity."xsd:string
http://purl.uniprot.org/uniprot/#_1743264163D8A738EDE6D18088DCC94CCD0D906F09105A6FF68A7271A827219A83ED7BA5179751ADEE761A893F414A21http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/CD0D48C9F484A66FA4E438CF1EB50B9A8CBAD2E47F08F2A03400AA8614FC832A52F8BC5F3B9B075AD403A23B642A81DA
http://purl.uniprot.org/uniprot/A0A0A1EII5http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/CD0D48C9F484A66FA4E438CF1EB50B9A8CBAD2E47F08F2A03400AA8614FC832A52F8BC5F3B9B075AD403A23B642A81DA
http://purl.uniprot.org/uniprot/#_A0A0A1EII5-mappedCitation-29136273http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/CD0D48C9F484A66FA4E438CF1EB50B9A8CBAD2E47F08F2A03400AA8614FC832A52F8BC5F3B9B075AD403A23B642A81DA