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- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion type Assertion NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_head.
- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_provenance.
- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion evidence source_evidence_literature NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_provenance.
- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion SIO_000772 19247433 NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_provenance.
- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion wasDerivedFrom befree-2016 NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_provenance.
- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion wasGeneratedBy ECO_0000203 NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_provenance.