Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion type Assertion NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_head.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion description "[Heterozygous mutations in GRN are a major cause of frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP), the second most common early-onset dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion evidence source_evidence_literature NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion SIO_000772 22608501 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion wasDerivedFrom befree-2016 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion wasGeneratedBy ECO_0000203 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.