Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_assertion description "[We report a new RET point mutation [R694Q (CGG-->CAG)], serendipitously found in a 23-yr-old woman with hypothyroidism due to atrophic Hashimoto's thyroiditis and primary ovarian failure, without altered calcitonin secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_assertion evidence source_evidence_literature NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_assertion SIO_000772 15472167 NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_assertion wasDerivedFrom befree-2016 NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_assertion wasGeneratedBy ECO_0000203 NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.
- befree-2016 importedOn "2016-02-19" NP463537.RAphu1ulM4k2d-OxcFYQXraf3NK_dJxU7qBFf5sxiYG78130_provenance.