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- source_evidence_literature type ECO_0000212 NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_assertion description "[We studied women at high risk of hereditary breast cancer syndromes who underwent testing for BRCA1 and BRCA2 to estimate DCIS prevalence and incidence in known BRCA-positive women compared with high-risk women who were mutation negative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_assertion evidence source_evidence_literature NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_assertion SIO_000772 17210933 NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_assertion wasDerivedFrom gad-20150221 NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_assertion wasGeneratedBy ECO_0000203 NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP104868.RAUISwZSr4zHedWGxH-RG4SZDgOOJvgDmSGnVCTSn9oh0130_provenance.