Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion type Assertion NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_head.
- NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion description "[The absence of pathogenic mutations in VSX1, SOD1, COL4A3, and COL4A4 genes in our large number of unrelated keratoconus patients indicates that other genetic factors are involved in the development of this disorder; nevertheless, a significant correlation of a few polymorphisms indicates that there could be a link between specific polymorphisms and KC disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_provenance.
- NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion evidence source_evidence_literature NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_provenance.
- NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion SIO_000772 20664914 NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_provenance.
- NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion wasDerivedFrom gad-20150221 NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_provenance.
- NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_assertion wasGeneratedBy ECO_0000203 NP182422.RAtpaqgsalvqH6BE6yT3axbwACdSlYOdNGyLpiAzF-ZbM130_provenance.