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DESCRIBE <http://purl.uniprot.org/SHA-384/C75EC8F749CDE90EB64CE0DDB0FA6534910197ABE473A62687F0A77D77117ACE5899DFFDCDE143204EA0462876473363>
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http://purl.uniprot.org/SHA-384/C75EC8F749CDE90EB64CE0DDB0FA6534910197ABE473A62687F0A77D77117ACE5899DFFDCDE143204EA0462876473363
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C75EC8F749CDE90EB64CE0DDB0FA6534910197ABE473A62687F0A77D77117ACE5899DFFDCDE143204EA0462876473363
http://www.w3.org/2000/01/rdf-schema#comment
"SMC1A mutation is associated with Cornelia de Lange syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_8C7BA359BA9D317A33D57785B8E67853FFD3E2AEF4934742E0206BAA34781B698FB119AD347D9CDED7C945E0C2319B7F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C75EC8F749CDE90EB64CE0DDB0FA6534910197ABE473A62687F0A77D77117ACE5899DFFDCDE143204EA0462876473363
http://purl.uniprot.org/uniprot/G8JLG1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C75EC8F749CDE90EB64CE0DDB0FA6534910197ABE473A62687F0A77D77117ACE5899DFFDCDE143204EA0462876473363
http://purl.uniprot.org/uniprot/#_G8JLG1-mappedCitation-29860495
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C75EC8F749CDE90EB64CE0DDB0FA6534910197ABE473A62687F0A77D77117ACE5899DFFDCDE143204EA0462876473363