Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_assertion description "[Logistic regression analysis of classic coronary risk factors and the genetic polymorphisms demonstrated that hypertension and ACE DD genotype were the most significant contributors to T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_assertion evidence source_evidence_literature NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_assertion SIO_000772 20580725 NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_assertion wasDerivedFrom gad-20150221 NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_assertion wasGeneratedBy ECO_0000203 NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP60682.RApu9cdQhbORMmsGd7A3x0xxzoZGI97f8T29_3DnF5xGA130_provenance.