Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion type Assertion NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_head.
- NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion description "[Dominant FBN1 mutations cause IEL or syndromic ectopia lentis (Marfan syndrome and Weill-Marchesani syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_provenance.
- NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion evidence source_evidence_literature NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_provenance.
- NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion SIO_000772 21989719 NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_provenance.
- NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion wasDerivedFrom befree-2016 NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_provenance.
- NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_assertion wasGeneratedBy ECO_0000203 NP930204.RAeysVIYd0Lx0Ywb0TG85bXlETcLCWRPNaY95x0Ugdum0130_provenance.