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- source_evidence_literature type ECO_0000212 NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_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." NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_assertion evidence source_evidence_literature NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_assertion SIO_000772 21862621 NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_assertion wasDerivedFrom befree-20150227 NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_assertion wasGeneratedBy ECO_0000203 NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.