Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_assertion> ?p ?o ?g. }
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- NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_assertion type Assertion NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_head.
- NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_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." NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_provenance.
- NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_assertion evidence source_evidence_literature NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_provenance.
- NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_assertion SIO_000772 17903294 NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_provenance.
- NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_assertion wasDerivedFrom gad-20150221 NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_provenance.
- NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_assertion wasGeneratedBy ECO_0000203 NP112623.RAkkNc2pFN_4f4-SO2ofTPWIocJgtjI0d4NYpQUCFIw28130_provenance.