Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion> ?p ?o ?g. }
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- NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion type Assertion NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_head.
- NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion description "[Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) is caused by mutations in Valosin-containing protein (VCP), a hexameric AAA ATPase that participates in a variety of cellular processes such as protein degradation, organelle biogenesis, and cell-cycle regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_provenance.
- NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion evidence source_evidence_literature NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_provenance.
- NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion SIO_000772 21304887 NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_provenance.
- NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion wasDerivedFrom befree-20140225 NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_provenance.
- NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_assertion wasGeneratedBy ECO_0000203 NP211981.RA9g3TgrnCxsqmakcRj0CQiK2fKA62wv7_KL6DtkCVbbY130_provenance.