Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_assertion description "[Residual VLCAD activity of 4 patients with confirmed VLCAD-deficiency was between 0.3 and 1.1%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_assertion evidence source_evidence_literature NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_assertion SIO_000772 19649258 NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_assertion wasDerivedFrom befree-2016 NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_assertion wasGeneratedBy ECO_0000203 NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.
- befree-2016 importedOn "2016-02-19" NP755009.RAiVXtD7YqCVYxU2hTcIhY9QEam1JTtThtPkaD20u1GsI130_provenance.