Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_assertion description "[The aim of the study was to evaluate the renin-angiotensin system and serotonin transporter gene polymorphisms in relation to hemodynamic parameters and heart rate variability during a head-up tilt test (HUT) in patients with vasovagal syncope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_assertion evidence source_evidence_literature NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_assertion SIO_000772 19067809 NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_assertion wasDerivedFrom befree-20140225 NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_assertion wasGeneratedBy ECO_0000203 NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP629783.RAg-OoyewHnDV0NgyopcXuvdmoT5Zx_grTjn6NTFuwKnk130_provenance.