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- source_evidence_literature type ECO_0000212 NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1187339.RA3GEhlHzPirsdee2IHKc8lDbo0SRaMMm9eysrg5dEYsk130_provenance.