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- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion type Assertion NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_head.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion wasGeneratedBy ECO_0000203 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion wasDerivedFrom befree-2016 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion SIO_000772 12798584 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion evidence source_evidence_literature NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion description "[Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.