Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_assertion type Assertion NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_head.
- NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_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." NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_provenance.
- NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_assertion evidence source_evidence_literature NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_provenance.
- NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_assertion SIO_000772 15732117 NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_provenance.
- NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_assertion wasDerivedFrom befree-20140225 NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_provenance.
- NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_assertion wasGeneratedBy ECO_0000203 NP758047.RAgksE_alzZboEN_OGLm9LsWrT9xVPpA93rKypUVeMvqg130_provenance.