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- NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_assertion type Assertion NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_head.
- NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_assertion description "[Mutations in the valosin-containing protein (VCP) gene on chromosome 9p13-p12 recently have been shown to cause autosomal dominant inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_provenance.
- NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_assertion evidence source_evidence_literature NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_provenance.
- NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_assertion SIO_000772 15732117 NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_provenance.
- NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_assertion wasDerivedFrom befree-20140225 NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_provenance.
- NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_assertion wasGeneratedBy ECO_0000203 NP776862.RA2KJwHBjQxvnI4fJo6kq0jdOKC0d6U_K8HKN5_HXOZEs130_provenance.