Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion description "[No significant associations were found. Within the limitations imposed by the size of the clinical sample, these findings suggest that the above polymorphic loci do not contribute significantly to risk for TD. Further examination of loci that yielded positive results at a trend level and investigation of other candidate genetic loci coding for antipsychotic drug targets is warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion evidence source_evidence_literature NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion SIO_000772 14583797 NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion wasDerivedFrom gad-20130706 NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion wasGeneratedBy ECO_0000203 NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance.