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- source_evidence_literature type ECO_0000212 NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion evidence source_evidence_literature NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion SIO_000772 12215251 NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion wasDerivedFrom befree-2016 NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion wasGeneratedBy ECO_0000203 NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- befree-2016 importedOn "2016-02-19" NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.