Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion type Assertion NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_head.
- NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_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." NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance.
- NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion evidence source_evidence_literature NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance.
- NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion SIO_000772 20664914 NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance.
- NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion wasDerivedFrom befree-20140225 NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance.
- NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion wasGeneratedBy ECO_0000203 NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance.