Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_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." NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_assertion evidence source_evidence_literature NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_assertion SIO_000772 20094846 NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_assertion wasDerivedFrom befree-2016 NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_assertion wasGeneratedBy ECO_0000203 NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.
- befree-2016 importedOn "2016-02-19" NP788794.RAzvjOy7Altnm93bEuUi--J3iMnABzxsdx1pwUSg3uiJM130_provenance.