Matches in Nanopublications for { ?s ?p "[Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP159511.RABw1Sd9S4sBFyBrQHPtRWep8riWTxXyWRSk7omQyabPA130_assertion description "[Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159511.RABw1Sd9S4sBFyBrQHPtRWep8riWTxXyWRSk7omQyabPA130_provenance.
- NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_assertion description "[Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- NP712421.RAT_w1T4TuVjoV0QSiB03hi3dTN0MNw2RQK8OP42RGkcY130_assertion description "[Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712421.RAT_w1T4TuVjoV0QSiB03hi3dTN0MNw2RQK8OP42RGkcY130_provenance.