Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_assertion description "[A significant association was observed for the TREM2 p.R47H substitution in susceptibility to frontotemporal dementia (OR = 5.06; p-value = 0.001) and Parkinson's disease (OR = 2.67; p-value = 0.026), while no evidence of association with risk of amyotrophic lateral sclerosis, progressive supranuclear palsy or ischemic stroke was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_assertion evidence source_evidence_literature NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_assertion SIO_000772 23800361 NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_assertion wasDerivedFrom befree-20140225 NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_assertion wasGeneratedBy ECO_0000203 NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939344.RA7vEnLhWKZI7FJE4axxQbO7ewwX3gCQtyXFGLBChMYd0130_provenance.