Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_assertion> ?p ?o ?g. }
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- NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_assertion type Assertion NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_head.
- NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_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." NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_provenance.
- NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_assertion evidence source_evidence_literature NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_provenance.
- NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_assertion SIO_000772 17903294 NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_provenance.
- NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_assertion wasDerivedFrom gad-20150221 NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_provenance.
- NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_assertion wasGeneratedBy ECO_0000203 NP112638.RAYnpQh7XappSsIdFdOaS1vVuNlm3cU5vuf0FVZEkJbv4130_provenance.