Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_assertion description "[The ALDH2 mutant was significantly associated with level of high-sensitivity C-reactive protein (hs-CRP) in patients with ACS (P = 0.002) and in controls (P = 0.009) and number of circulating endothelial progenitor cells (EPCs) (P = 0.032); furthermore, inclusion of hs-CRP level and EPCs number as independent variables in regression analysis reduced the importance of ALDH2 polymorphism in ACS or primary STEMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_assertion evidence source_evidence_literature NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_assertion SIO_000772 21958412 NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_assertion wasDerivedFrom befree-20150227 NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_assertion wasGeneratedBy ECO_0000203 NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP234791.RAc-tdBbMbW1h8aot-4P0JVUAQC_YrTnARg5RK_WTMQOU130_provenance.