Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_assertion description "[The K allele of the R219K variant was significantly more frequent in FH subjects without premature CHD (0.32, 95% CI 0.27 to 0.37) than in FH subjects with premature CHD (0.25, 95% CI 0.21 to 0.29) (p<0.05), suggesting that the genetic variant R219K in AB]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_assertion evidence source_evidence_literature NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_assertion SIO_000772 12624133 NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_assertion wasDerivedFrom gad-20150221 NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_assertion wasGeneratedBy ECO_0000203 NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.
- gad-20150221 importedOn "2015-02-21" NP78650.RAmcWhD4BOcCaCsriywHxjtY3aQCwsy7uSRXHiFFG449M130_provenance.