Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_assertion description "[BRCA1 and BRCA2 screening in women at high-risk of breast cancer results in the identification of both unambiguously defined deleterious mutations and sequence variants of unknown clinical significance (VUS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_assertion evidence source_evidence_literature NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_assertion SIO_000772 20104584 NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_assertion wasDerivedFrom befree-2016 NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_assertion wasGeneratedBy ECO_0000203 NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.
- befree-2016 importedOn "2016-02-19" NP789779.RACCFEo7bjR6r4Hr6SRGzOOSKYnpsNyVlRytoYHUmK53A130_provenance.