Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_assertion description "[No association was found either between the factor V point mutation (1691G-A) or the RR genotype of the factor VII Arg/Gln353 gene polymorphism and the risk of ACI using univariate analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_assertion evidence source_evidence_literature NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_assertion SIO_000772 12859287 NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_assertion wasDerivedFrom befree-20140225 NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_assertion wasGeneratedBy ECO_0000203 NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP912878.RAFeWLlq8xN43KzCd_MwYMEnKwyhpIgohYtTGCGCcdoN0130_provenance.