Matches in Nanopublications for { ?s ?p "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257514.RAbU0lqUJ6POy4M-SCChIPxkIHK35YWOLN10EJVu6XE44130_provenance.
- NP420412.RAA0yoj6taI9zIvP7bStwP8rodcP0FFf3SgLhD8KZdR4U130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420412.RAA0yoj6taI9zIvP7bStwP8rodcP0FFf3SgLhD8KZdR4U130_provenance.
- assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP988972.RAeUNYSrfmZLwXZVSqDpGGSw7lt_L6UZd-1sQUPmYv2NY130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988972.RAeUNYSrfmZLwXZVSqDpGGSw7lt_L6UZd-1sQUPmYv2NY130_provenance.
- NP768738.RAjSzlskQvUu_JcAMsa13SraY0Rliwaj2DDZpQsYsDf8k130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768738.RAjSzlskQvUu_JcAMsa13SraY0Rliwaj2DDZpQsYsDf8k130_provenance.
- NP988975.RACO3_VgBF2M5_wqBmEeKuu0vH5xJbWOmtIcLq3QgbgpY130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988975.RACO3_VgBF2M5_wqBmEeKuu0vH5xJbWOmtIcLq3QgbgpY130_provenance.
- NP988971.RAkYAqNIAchGQUGIaoy0Ad5Y4-eGlSn5tWwQxXMt1IZX4130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988971.RAkYAqNIAchGQUGIaoy0Ad5Y4-eGlSn5tWwQxXMt1IZX4130_provenance.
- NP988973.RAEvbuZXMsbcWinMOb4zH5yHppMghKJ0cMH46sqmvjL8M130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988973.RAEvbuZXMsbcWinMOb4zH5yHppMghKJ0cMH46sqmvjL8M130_provenance.
- NP768944.RAFhsoyo-yE0xRHYKOJLiC8X9LDxP0s4hmOkSqZmVXgrY130_assertion description "[Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768944.RAFhsoyo-yE0xRHYKOJLiC8X9LDxP0s4hmOkSqZmVXgrY130_provenance.