Matches in Nanopublications for { ?s ?p "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP768866.RAvnsSfM28BoT22ucBGqDZgWovGDJxudOtS6hb5bRB9_Q130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768866.RAvnsSfM28BoT22ucBGqDZgWovGDJxudOtS6hb5bRB9_Q130_provenance.
- NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_provenance.
- NP1242238.RAtoITqcT34Neuvuik4P59l_YxUw9nJHFYZN3LXPONLKs130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242238.RAtoITqcT34Neuvuik4P59l_YxUw9nJHFYZN3LXPONLKs130_provenance.
- NP1242242.RAg6-fqz9IYDY-Sq86OrkgoyeECk-IIw806vYNWtxhWgs130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242242.RAg6-fqz9IYDY-Sq86OrkgoyeECk-IIw806vYNWtxhWgs130_provenance.
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