Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion type Assertion NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_head.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_provenance.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion evidence source_evidence_literature NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_provenance.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion SIO_000772 21858451 NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_provenance.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion wasDerivedFrom befree-20140225 NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_provenance.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion wasGeneratedBy ECO_0000203 NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_provenance.