Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_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." NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_assertion evidence source_evidence_literature NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_assertion SIO_000772 11502905 NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_assertion wasDerivedFrom befree-20140225 NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_assertion wasGeneratedBy ECO_0000203 NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217299.RAiNz3lRo5W-0EfcWAEESkKrPIIYI2oqaZSBTBu46YEu0130_provenance.