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- NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_assertion type Assertion NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_head.
- NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_assertion wasGeneratedBy ECO_0000203 NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_provenance.
- NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_assertion wasDerivedFrom befree-20150227 NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_provenance.
- NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_assertion SIO_000772 18499664 NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_provenance.
- NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_assertion evidence source_evidence_literature NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_provenance.
- NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_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." NP676359.RAzs7pbZyRZWC_0D-DJ5EEBPn18V0y3tB_YDrnNpw6v3E130_provenance.