Matches in Nanopublications for { ?s ?p "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 14 of
14
with 100 items per page.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_provenance.
- NP148867.RAuJxcr6kdxWCy2hluvdqTAZv-YhFLvepGKTRox3oHI-8130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148867.RAuJxcr6kdxWCy2hluvdqTAZv-YhFLvepGKTRox3oHI-8130_provenance.
- NP141010.RAlScFruTGd-lLzIlgfdveU1qyRmehazLWvGOI1GnaQ8o130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141010.RAlScFruTGd-lLzIlgfdveU1qyRmehazLWvGOI1GnaQ8o130_provenance.
- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP204154.RA_kVK8YlH4R_-2MNoEvrhXuIThrmfo0wrI6g5HLSbiWQ130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204154.RA_kVK8YlH4R_-2MNoEvrhXuIThrmfo0wrI6g5HLSbiWQ130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP211992.RAH_2TUMNWb5cwoUT0YR6GcykjeqcSVMv7GGmp1B0AXEE130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211992.RAH_2TUMNWb5cwoUT0YR6GcykjeqcSVMv7GGmp1B0AXEE130_provenance.
- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_provenance.
- assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP224572.RApQxgYTxpdY_wvRRbBHTDXsjU-Htk9XeBoA36xTAcpTA130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224572.RApQxgYTxpdY_wvRRbBHTDXsjU-Htk9XeBoA36xTAcpTA130_provenance.