Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_assertion description "[The large effects observed for DRD2/ANKK1 might be related to our study design, in which individual therapy was decided by the physician. Further studies are needed to clarify the genetic effects of DRD2/ANKK1 especially in eal-life settings outside clinical trials.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_assertion evidence source_evidence_literature NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_assertion SIO_000772 20350135 NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_assertion wasDerivedFrom gad-20130706 NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_assertion wasGeneratedBy ECO_0000203 NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP75749.RAC2ggLbdjbrzSMNVlUETtSqQTyBeHht3wICwlNr1ZKqU130_provenance.