Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion> ?p ?o ?g. }
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- NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion type Assertion NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_head.
- NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion description "[The evidences of our investigations show that MLH1 and MSH2 gene mutations have an equivalent etiopathological role both for Lynch syndrome and for MTS; hence, we propose a broadened clinical criteria for definition of Lynch syndrome that will include sebaceous adenoma, carcinoma, and keratoacanthoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_provenance.
- NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion evidence source_evidence_literature NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_provenance.
- NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion SIO_000772 16826164 NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_provenance.
- NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion wasDerivedFrom befree-2016 NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_provenance.
- NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_assertion wasGeneratedBy ECO_0000203 NP558718.RApM_mUJGOtfagxQCH73LcY-rBAsBF-YWHzJOgAmpFgds130_provenance.