Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion> ?p ?o ?g. }
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- NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion type Assertion NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_head.
- NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion description "[Almost 90% of the MODY cases in the group studied are explained by mutations in the major genes GCK (MODY2) and HNF-1alpha (MODY3), although differences in the relative prevalence of each form could be partly due to patient referral bias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_provenance.
- NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion evidence source_evidence_literature NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_provenance.
- NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion SIO_000772 17573900 NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_provenance.
- NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion wasDerivedFrom lhgdn-20090331 NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_provenance.
- NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_assertion wasGeneratedBy ECO_0000203 NP226327.RAXpBperl8AHxEP7Z9FtFXddiQv-uFlD7faXQv5ZpD8m8130_provenance.