Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_assertion description "[Germline mutations of RET cause a dominantly inherited dysgenesis of the enteric nervous system known as Hirschsprung's disease (HSCR; aganglionosis megacolon).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_assertion evidence source_evidence_literature NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_assertion SIO_000772 10484767 NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_assertion wasDerivedFrom befree-20150227 NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_assertion wasGeneratedBy ECO_0000203 NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP670727.RAxH8LWrNcQXiH4nM2nQLfs8rYiQc6Dql37MWaL58zVkA130_provenance.