Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_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." NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_assertion evidence source_evidence_literature NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_assertion SIO_000772 21958412 NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_assertion wasDerivedFrom befree-20140225 NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_assertion wasGeneratedBy ECO_0000203 NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP257352.RANnXDcNhHYa1VHkNbbUqUGUYX8vzMQ6-hdCePlWU4-3Q130_provenance.