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- NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_assertion type Assertion NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_head.
- NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_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." NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_provenance.
- NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_assertion evidence source_evidence_literature NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_provenance.
- NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_assertion SIO_000772 20094846 NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_provenance.
- NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_assertion wasDerivedFrom befree-2016 NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_provenance.
- NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_assertion wasGeneratedBy ECO_0000203 NP788796.RAraQUB1XY4DEu0Tkpefh9e_By69oXOOUvDU8AYrt_EVY130_provenance.