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- NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion type Assertion NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_head.
- NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion wasGeneratedBy ECO_0000203 NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance.
- NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion wasDerivedFrom befree-2016 NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance.
- NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion SIO_000772 18726931 NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance.
- NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion evidence source_evidence_literature NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance.
- NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_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." NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance.