Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion> ?p ?o ?g. }
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- NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion type Assertion NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_head.
- NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion wasGeneratedBy ECO_0000203 NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_provenance.
- NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion wasDerivedFrom gad-20150221 NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_provenance.
- NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion SIO_000772 12446192 NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_provenance.
- NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion evidence source_evidence_literature NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_provenance.
- NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_assertion description "[ An increasing number of risk alleles are associated with an elevated risk for CAD. An analysis of multiple polymorphisms, some several hundred, each with a small impact, may allow improved assessment of the individual genetic burden for CAD. Larger studi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77218.RAVseyQe-TH9qXdytrVg_QtNxz7hy5WzMNWBKy1W9jtgU130_provenance.