Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_assertion type Assertion NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_head.
- NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_assertion wasGeneratedBy ECO_0000203 NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_provenance.
- NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_assertion wasDerivedFrom gad-20150221 NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_provenance.
- NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_assertion SIO_000772 12446192 NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_provenance.
- NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_assertion evidence source_evidence_literature NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_provenance.
- NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_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." NP56652.RAlthVQi3iVpC9Kt1GzMDcgzKZ6iuwAYxrJMmSlQYsBHs130_provenance.