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- NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion type Assertion NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_head.
- NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_provenance.
- NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion evidence source_evidence_literature NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_provenance.
- NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion SIO_000772 21862621 NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_provenance.
- NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion wasDerivedFrom befree-2016 NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_provenance.
- NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion wasGeneratedBy ECO_0000203 NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_provenance.