Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP122972.RA4Xf9cHm1EfGuuYT1TVNYkT1rfPfC2db7JC3k_81BVp8#assertion> ?p ?o ?g. }
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- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 18726931 provenance.
- assertion evidence source_evidence_literature provenance.
- 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." provenance.