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- NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion type Assertion NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_head.
- NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion wasGeneratedBy ECO_0000203 NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_provenance.
- NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion wasDerivedFrom befree-2016 NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_provenance.
- NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion SIO_000772 18499664 NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_provenance.
- NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion evidence source_evidence_literature NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_provenance.
- NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672831.RAi5eU4EDLXMf9_8cKFPvMA4FaJXaS4UYFMkXiI1hK8VM130_provenance.