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- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion type Assertion NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_head.
- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_provenance.
- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion evidence source_evidence_literature NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_provenance.
- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion SIO_000772 18765513 NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_provenance.
- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion wasDerivedFrom befree-20140225 NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_provenance.
- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion wasGeneratedBy ECO_0000203 NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_provenance.