Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_assertion description "[We did not find main effects of the COMT and SLC6A2 NET1 gene haplotypes on any ADHD symptom severity score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_assertion evidence source_evidence_literature NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_assertion SIO_000772 17994190 NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_assertion wasDerivedFrom befree-2016 NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_assertion wasGeneratedBy ECO_0000203 NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.
- befree-2016 importedOn "2016-02-19" NP639719.RAPJQmf1asxs9dwm8M3cmyFmWfWTMH6Xz_OUIkiVELmzc130_provenance.