Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion> ?p ?o ?g. }
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- NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion type Assertion NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_head.
- NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion description "[Inclusion body myopathy with Paget disease of the bone (PDB) and/or frontotemporal dementia (IBMPFD, OMIM 167320), is a progressive autosomal dominant disorder caused by mutations in the Valousin-containing protein (VCP, p97 or CDC48) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_provenance.
- NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion evidence source_evidence_literature NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_provenance.
- NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion SIO_000772 18260132 NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_provenance.
- NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion wasDerivedFrom befree-20150227 NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_provenance.
- NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_assertion wasGeneratedBy ECO_0000203 NP898183.RARi2jzeFQiVE2VZmgWQNuiQxVfkZKRPfhBOot085Ce1w130_provenance.