Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_assertion description "[We studied the replication error (RER) phenotype in noncoding (Bat-26, Bat-25, D2S123, D5S346, and D17S250) and coding (MSH3, MSH6, BAX, and TGFBR2 genes) DNA sequences, and characterized the germline and somatic mutations of the MSH2 gene in the tumors described above and in endometrial carcinomas from two of her affected siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_assertion evidence source_evidence_literature NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_assertion SIO_000772 15350299 NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_assertion wasDerivedFrom befree-20140225 NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_assertion wasGeneratedBy ECO_0000203 NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP778155.RApg1uIN9lr9FX5L8piGXhCAwNJ4iMW82Y1EjwFegaKQ0130_provenance.