Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion> ?p ?o ?g. }
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- NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion type Assertion NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_head.
- NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion description "[Using genome-wide association methodology, we have successfully identified a SNP in complete LD with a sequence variant previously shown to be strongly associated with factor VII, providing proof of principle for this approach. Further study of additional]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_provenance.
- NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion evidence source_evidence_literature NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_provenance.
- NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion SIO_000772 17903294 NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_provenance.
- NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion wasDerivedFrom gad-20150221 NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_provenance.
- NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_assertion wasGeneratedBy ECO_0000203 NP156586.RALZYXObwl61VqLNviC8J3trh0W-fRl5LuiGVeEQPJM2U130_provenance.