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DESCRIBE <http://purl.uniprot.org/SHA-384/02E257C26DE7659012F52ACBD9C078FD49A1860050A49341EB9E9F8819A77863AB7336AB40FEDEFD96A65077D370E7B6>
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http://purl.uniprot.org/SHA-384/02E257C26DE7659012F52ACBD9C078FD49A1860050A49341EB9E9F8819A77863AB7336AB40FEDEFD96A65077D370E7B6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/02E257C26DE7659012F52ACBD9C078FD49A1860050A49341EB9E9F8819A77863AB7336AB40FEDEFD96A65077D370E7B6
http://www.w3.org/2000/01/rdf-schema#comment
"GDI1 mutations cause an unspecific phenotype characterized by cognitive deficits of variable degree in males and to a lesser degree in female carriers."
xsd:string
http://purl.uniprot.org/uniprot/#_B97E5FA2B317CFB9594AF7B87409E73D7C086AFFAEDD58E871FC5660ACCDF1A082EB72C22835C35D88DB3BE68743DF7E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/02E257C26DE7659012F52ACBD9C078FD49A1860050A49341EB9E9F8819A77863AB7336AB40FEDEFD96A65077D370E7B6
http://purl.uniprot.org/uniprot/B4E070
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/02E257C26DE7659012F52ACBD9C078FD49A1860050A49341EB9E9F8819A77863AB7336AB40FEDEFD96A65077D370E7B6
http://purl.uniprot.org/uniprot/#_B4E070-mappedCitation-22002931
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/02E257C26DE7659012F52ACBD9C078FD49A1860050A49341EB9E9F8819A77863AB7336AB40FEDEFD96A65077D370E7B6