Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_assertion description "[We conducted a three-stage case-control study of CHD in Chinese to test our hypothesis by genotyping miR-196a2 rs11614913 and three other pre-miRNA SNPs (miR-146a rs2910164, miR-149 rs2292832, and miR-499 rs3746444) in 1,324 CHD cases and 1,783 non-CHD controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_assertion evidence source_evidence_literature NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_assertion SIO_000772 19514064 NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_assertion wasDerivedFrom befree-20150227 NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_assertion wasGeneratedBy ECO_0000203 NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP994513.RAO-ftVx3EYCee2C_FwE7QXRkQwdMZY0A-wvaP5UTFz8w130_provenance.