Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_assertion description "[To investigate catecholamine phenotypes and the effects of a tyrosine hydroxylase inhibitor in individuals with the 22q11.2 deletion syndrome and low-activity catechol-O-methyltransferase (COMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_assertion evidence source_evidence_literature NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_assertion SIO_000772 11502905 NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_assertion wasDerivedFrom befree-20150227 NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_assertion wasGeneratedBy ECO_0000203 NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP735354.RAlxBxymkh8a5MqUFWPMlVJ8l9Otz4Dweqi8R-wdAFMZs130_provenance.