Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion> ?p ?o ?g. }
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- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion type Assertion NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_head.
- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_provenance.
- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion evidence source_evidence_literature NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_provenance.
- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion SIO_000772 22686199 NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_provenance.
- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion wasDerivedFrom befree-20140225 NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_provenance.
- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion wasGeneratedBy ECO_0000203 NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_provenance.