Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_assertion description "[In a large case-control study of 1425 individuals who survived a myocardial infarction prior to age 45, the N700S polymorphism was a significant risk factor for myocardial infarction in both homozygous (odds ratio [OR] 1.9, 95% confidence interval [CI] 1.1-3.3, P = .01) and heterozygous carriers of the S700 allele (OR 1.4, 95% CI 1.1-3.3, P = .01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_assertion evidence source_evidence_literature NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_assertion SIO_000772 16684956 NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_assertion wasDerivedFrom befree-20150227 NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_assertion wasGeneratedBy ECO_0000203 NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP991143.RAv4m8eRuIV9xeOFgzlnp9sP9rQ7ybNp-TPvM9JlQo9BE130_provenance.