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- NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_assertion type Assertion NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_head.
- NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_assertion description "[Fragile X syndrome (FXS) is the most common inherited form of intellectual disability caused by the CGG trinucleotide expansion in the 3'-untranslated region of the FMR1 gene on the X chromosome, that silences the expression of the Fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_provenance.
- NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_assertion evidence source_evidence_literature NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_provenance.
- NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_assertion SIO_000772 25406362 NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_provenance.
- NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_assertion wasDerivedFrom befree-2016 NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_provenance.
- NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_assertion wasGeneratedBy ECO_0000203 NP1238353.RAgwryFUKgi3mKZDKYSMq8SjeX9fgdFTswivpnZ3W98fM130_provenance.