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- NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_assertion type Assertion NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_head.
- NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_assertion description "[De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_provenance.
- NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_assertion evidence source_evidence_literature NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_provenance.
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- NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_assertion wasDerivedFrom befree-2016 NP1230452.RA1EU_XyaVxjGKjgfSWLh8CEEa5WlMZxuLQromOy9CYNA130_provenance.
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