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- NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_assertion type Assertion NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_head.
- NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_assertion description "[Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_provenance.
- NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_assertion evidence source_evidence_literature NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_provenance.
- NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_assertion SIO_000772 20094846 NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_provenance.
- NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_assertion wasDerivedFrom befree-20150227 NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_provenance.
- NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_assertion wasGeneratedBy ECO_0000203 NP404906.RAHUbALoCraNWRzg_1DT4kgLKcQqWhgg0O_jc4BdI8-2Q130_provenance.