Matches in Nanopublications for { ?s ?p "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_provenance.
- NP598269.RAfMMHSbaAhNJY95QPTa5yLXMQE8lE7aABVtKJThAxJjY130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598269.RAfMMHSbaAhNJY95QPTa5yLXMQE8lE7aABVtKJThAxJjY130_provenance.
- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_provenance.
- NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- NP339434.RAV6Yf9ZVaL8cPLEgHv51KMn2qewUB5MR-Vkee5B8w4II130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339434.RAV6Yf9ZVaL8cPLEgHv51KMn2qewUB5MR-Vkee5B8w4II130_provenance.
- assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP835145.RAN4xvYyAyke4bmOIGc4utOebNHS08G_GY5ta0ZZ8tmcY130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835145.RAN4xvYyAyke4bmOIGc4utOebNHS08G_GY5ta0ZZ8tmcY130_provenance.