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- NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_assertion type Assertion NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_head.
- NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_assertion wasGeneratedBy ECO_0000203 NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_provenance.
- NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_assertion wasDerivedFrom befree-20150227 NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_provenance.
- NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_assertion SIO_000772 22998673 NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_provenance.
- NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_assertion evidence source_evidence_literature NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_provenance.
- NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_assertion description "[It is now clearly emerging that epilepsy has distinctive characteristics in typical Rett syndrome and in the different syndromes caused by CDKL5 and FOXG1 gene alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719282.RAP400rzwdQHKfXDaFr3ddtKE78Xk3vQMLVJGxc5YyZZg130_provenance.