Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion type Assertion NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_head.
- NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion description "[Variants identified through this study were previously reported to be involved in FTD and/or MND, but we are the first to describe their effects as potential disease modifiers in the presence of a clear pathogenic mutation (i.e.C9ORF72 repeat expansion).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_provenance.
- NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion evidence source_evidence_literature NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_provenance.
- NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion SIO_000772 25239657 NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_provenance.
- NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion wasDerivedFrom befree-2016 NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_provenance.
- NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_assertion wasGeneratedBy ECO_0000203 NP1222098.RAfbe5FqZIl3dJKLSByMSGfHt5DbbxZ0BtG5qam802JyA130_provenance.