Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_assertion type Assertion NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_head.
- NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_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." NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_provenance.
- NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_assertion evidence source_evidence_literature NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_provenance.
- NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_assertion SIO_000772 17903294 NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_provenance.
- NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_assertion wasDerivedFrom gad-20150221 NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_provenance.
- NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_assertion wasGeneratedBy ECO_0000203 NP156567.RAlv1k4H3nCgFP3kmRWZZBi6jM4EIlVUxYHsms_1d2r4Q130_provenance.