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DESCRIBE <http://purl.uniprot.org/SHA-384/54C8786AF3E3E5C1DFAB889781BC875D6ACB19ADADD234F061B005746FA1B80D50681D84637280405B3E691EB7DA7CAA>
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http://purl.uniprot.org/SHA-384/54C8786AF3E3E5C1DFAB889781BC875D6ACB19ADADD234F061B005746FA1B80D50681D84637280405B3E691EB7DA7CAA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/54C8786AF3E3E5C1DFAB889781BC875D6ACB19ADADD234F061B005746FA1B80D50681D84637280405B3E691EB7DA7CAA
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in ACTB cause a distinctly more severe phenotype than ACTG1 mutations in Baraitser-Winter syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_A7C107669EA03801F5F4C371AE9538D8F0AAD6374A2D513E8E1E924418502DEEA9DCFDBF2641E28DC67A36DCA9608BE9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/54C8786AF3E3E5C1DFAB889781BC875D6ACB19ADADD234F061B005746FA1B80D50681D84637280405B3E691EB7DA7CAA
http://purl.uniprot.org/uniprot/Q6PJ43
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/54C8786AF3E3E5C1DFAB889781BC875D6ACB19ADADD234F061B005746FA1B80D50681D84637280405B3E691EB7DA7CAA
http://purl.uniprot.org/uniprot/#_Q6PJ43-mappedCitation-23756437
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/54C8786AF3E3E5C1DFAB889781BC875D6ACB19ADADD234F061B005746FA1B80D50681D84637280405B3E691EB7DA7CAA