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- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_assertion type Assertion NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_head.
- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_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." NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_assertion evidence source_evidence_literature NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_assertion SIO_000772 18765513 NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_assertion wasDerivedFrom befree-2016 NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_assertion wasGeneratedBy ECO_0000203 NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.