Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_assertion description "[Our findings suggest that the genetic variations in the ADRA1A gene are significantly associated with essential hypertension, and may play an important role in the development of essential hypertension in this Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_assertion evidence source_evidence_literature NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_assertion SIO_000772 16685204 NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_assertion wasDerivedFrom befree-20140225 NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_assertion wasGeneratedBy ECO_0000203 NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890436.RAONlJtGbCtPZMMfQ6OLXtgnNBXWrD-mb0Ni29Ns622WM130_provenance.