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- source_evidence_literature type ECO_0000212 NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_assertion description "[Mutations in FOXE3 are associated with both recessive and dominant inheritance of severe anterior ocular malformations and glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_assertion evidence source_evidence_literature NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_assertion SIO_000772 25504734 NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_assertion wasDerivedFrom befree-2016 NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_assertion wasGeneratedBy ECO_0000203 NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248079.RADfh_9-tk0PUEnGG8Tp9FDFdEAEsg7ZsLIO-Imtn9fj0130_provenance.