Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_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." NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_assertion evidence source_evidence_literature NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_assertion SIO_000772 17994190 NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_assertion wasDerivedFrom befree-20150227 NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_assertion wasGeneratedBy ECO_0000203 NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP816196.RA3XK6gB2z-BnswJSTNyG3r7BnVJ5v3oJl8Snzw1uVMeQ130_provenance.