Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion> ?p ?o ?g. }
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- NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion type Assertion NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_head.
- NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion wasGeneratedBy ECO_0000203 NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_provenance.
- NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion wasDerivedFrom befree-2016 NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_provenance.
- NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion SIO_000772 20519548 NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_provenance.
- NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion evidence source_evidence_literature NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_provenance.
- NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is a dominantly inherited degenerative disorder caused by mutations in the valosin-containing protein (VCP7) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816239.RA_bCuHId_C2fFErL39FoX9-3VTVxMqknA9qu2jlcjuYk130_provenance.