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- source_evidence_literature type ECO_0000212 NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_assertion description "[The FOXE1 gene was screened for mutations in a cohort of 34 unrelated patients with congenital hypothyroidism, 14 of whom had thyroid dysgenesis and 18 were normal (the thyroid status for 2 patients was unknown).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_assertion evidence source_evidence_literature NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_assertion SIO_000772 20094846 NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_assertion wasDerivedFrom befree-20150227 NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_assertion wasGeneratedBy ECO_0000203 NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404876.RA8H3uEK5zj1liqor3R2-zNyh3zby1H9KnbBfcbUzXrSc130_provenance.