Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_assertion description "[The mean concentration of FIXP was markedly reduced to 22.7 pmol/L in nine patients with hereditary factor VII deficiency (factor VII coagulant activity less than 7%) but was not significantly different from normal controls in nine subjects with factor XI deficiency (factor XI coagulant activity less than 8%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_assertion evidence source_evidence_literature NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_assertion SIO_000772 2383653 NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_assertion wasDerivedFrom befree-20150227 NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_assertion wasGeneratedBy ECO_0000203 NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392059.RAat_w8I6OLmePlHOQp5oELZJ0TJoiWY8M3gEcf4EHMZY130_provenance.