Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_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." NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_assertion evidence source_evidence_literature NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_assertion SIO_000772 2383653 NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_assertion wasDerivedFrom befree-20150227 NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_assertion wasGeneratedBy ECO_0000203 NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392151.RAFtgR2HM1nyRNAv6yTlQ8RpACoDrHl89Q9ppDpwO-63Y130_provenance.