Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_assertion description "[Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_assertion evidence source_evidence_literature NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_assertion SIO_000772 17994190 NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_assertion wasDerivedFrom gad-20130706 NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_assertion wasGeneratedBy ECO_0000203 NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51602.RAye6bdpAFC6-8PqFg2QRgaFsjMmLudcTA0sukpbYa9xA130_provenance.