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- NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_assertion type Assertion NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_head.
- NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_assertion wasGeneratedBy ECO_0000203 NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_provenance.
- NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_assertion wasDerivedFrom befree-20140225 NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_provenance.
- NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_assertion SIO_000772 18499664 NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_provenance.
- NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_assertion evidence source_evidence_literature NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_provenance.
- NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_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." NP181968.RAU1pmZflz9NhYeej4QIFsFg_g0iqicJIBPY3M0et_8OQ130_provenance.