Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_assertion> ?p ?o ?g. }
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- NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_assertion type Assertion NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_head.
- NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_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." NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_provenance.
- NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_assertion evidence source_evidence_literature NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_provenance.
- NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_assertion SIO_000772 20094846 NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_provenance.
- NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_assertion wasDerivedFrom gad-20150221 NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_provenance.
- NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_assertion wasGeneratedBy ECO_0000203 NP52024.RA3MxI5tjHH5Z-UVx7ea63t2MIhnKzOQJFCxpZ-KTSdZA130_provenance.