Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion type Assertion NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_head.
- NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion wasGeneratedBy ECO_0000203 NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance.
- NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion wasDerivedFrom befree-2016 NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance.
- NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion SIO_000772 18726931 NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance.
- NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion evidence source_evidence_literature NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance.
- NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion description "[Mutations in FOXL2 are known to cause blepharophimosis syndrome (BPES), an autosomal dominant eyelid malformation associated (type I) or not (type II) with ovarian dysfunction, leading to premature ovarian failure (POF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance.