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- source_evidence_literature type ECO_0000212 NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_assertion wasGeneratedBy ECO_0000203 NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_assertion wasDerivedFrom befree-20150227 NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_assertion SIO_000772 23326532 NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_assertion evidence source_evidence_literature NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.
- NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_assertion description "[Unconditional logistic regression showed that no significant association between common variants in the coding region of ROCK2 and CAD was observed in our study (for rs978906, OR = 0.92, 95% CI 0.72-1.20 and P = 0.63; for rs2230774, OR = 0.90, 95% CI 0.70-1.16 and P = 0.47; for rs56304104, OR = 0.97, 95% CI 0.70-1.31 and P = 0.83; respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824582.RA_bwx_vBTbD3D3QsiE5St0v-XnE4A0nMW-FpZJ_WkBgM130_provenance.