Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion> ?p ?o ?g. }
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- NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion type Assertion NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_head.
- NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion wasGeneratedBy ECO_0000203 NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_provenance.
- NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion wasDerivedFrom befree-2016 NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_provenance.
- NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion SIO_000772 19923742 NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_provenance.
- NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion evidence source_evidence_literature NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_provenance.
- NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_assertion description "[Mutations in p97 have been implicated in patients with inclusion-body myopathy associated with Paget's disease of the bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776603.RAcT3lOhEbDrZt5GKVg7i0KfE2JlrOGx1GY7Q2IRwV6wU130_provenance.