Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion> ?p ?o ?g. }
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- NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion type Assertion NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_head.
- NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion description "[Moreover, the detection of the TP53 R337H variant in our series and the fact that this variant has a founder effect in our population prompted us to suggest that all female breast cancer patients with clinical criteria for HBOC and negative for BRCA1/2 genes should be tested for the TP53 R337H variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion evidence source_evidence_literature NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion SIO_000772 24884479 NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion wasDerivedFrom befree-2016 NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_assertion wasGeneratedBy ECO_0000203 NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.