Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion description "[Our findings suggest that hypertension candidate gene variation may influence BP responses to specific antihypertensive drug therapies and measurement of genetic variation may assist in identifying subgroups of hypertensive patients who will benefit most from particular antihypertensive drug therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion evidence source_evidence_literature NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion SIO_000772 17854487 NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion wasDerivedFrom gad-20130706 NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion wasGeneratedBy ECO_0000203 NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.