Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.