Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion> ?p ?o ?g. }
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- NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion type Assertion NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_head.
- NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion description "[Here we expand the role of GRN in FTLD-U and demonstrate that a common genetic variant (rs5848), located in the 3'-untranslated region (UTR) of GRN in a binding-site for miR-659, is a major susceptibility factor for FTLD-U.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_provenance.
- NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion evidence source_evidence_literature NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_provenance.
- NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion SIO_000772 18723524 NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_provenance.
- NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion wasDerivedFrom befree-20140225 NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_provenance.
- NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_assertion wasGeneratedBy ECO_0000203 NP667105.RAnyLodRNi6rmxaH40SjCh-Pyo__1QtBev1yD2RqEQ1SQ130_provenance.