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- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion type Assertion NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_head.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion description "[Here, we identified two de novo mutations in patients with sporadic SCZ in GRIN2A and one de novo mutation in GRIN2B in a patient with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion evidence source_evidence_literature NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion SIO_000772 22833210 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion wasDerivedFrom befree-20150227 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.
- NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_assertion wasGeneratedBy ECO_0000203 NP434517.RAmhNqtrTsIs6HeYvnHhzpJppznEcGwdndBjx7P_qBjcI130_provenance.