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- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_assertion type Assertion NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_head.
- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_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." NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_provenance.
- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_assertion evidence source_evidence_literature NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_provenance.
- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_assertion SIO_000772 19247433 NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_provenance.
- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_assertion wasDerivedFrom befree-20150227 NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_provenance.
- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_assertion wasGeneratedBy ECO_0000203 NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_provenance.