Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_assertion type Assertion NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_head.
- NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_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." NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_provenance.
- NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_assertion evidence source_evidence_literature NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_provenance.
- NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_assertion SIO_000772 17903294 NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_provenance.
- NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_assertion wasDerivedFrom gad-20150221 NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_provenance.
- NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_assertion wasGeneratedBy ECO_0000203 NP156588.RAXnIrS_m7XkPQXOqJVLPoumKDnAYPcS2b0pkVfK2tjiM130_provenance.