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- source_evidence_literature type ECO_0000212 NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion evidence source_evidence_literature NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion SIO_000772 15734952 NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion wasDerivedFrom befree-20150227 NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion wasGeneratedBy ECO_0000203 NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.