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- source_evidence_literature type ECO_0000212 NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_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." NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_assertion evidence source_evidence_literature NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_assertion SIO_000772 17903294 NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_assertion wasDerivedFrom gad-20150221 NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_assertion wasGeneratedBy ECO_0000203 NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP112605.RAtg3UMM1ZUjIr1Di_mw5PBtH_ea99yeCdyEU38-GWlZE130_provenance.