Matches in Nanopublications for { ?s ?p "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion description "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_provenance.
- NP896305.RAyT0sPKedWcZUwQxrMK5kG4RYpOj-LAew2xdOORI35ns130_assertion description "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896305.RAyT0sPKedWcZUwQxrMK5kG4RYpOj-LAew2xdOORI35ns130_provenance.
- NP236677.RA0bhH2VGoSNbgpaU-JOZbOwmspNf4Nz_Gd_9_Xt6nEig130_assertion description "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236677.RA0bhH2VGoSNbgpaU-JOZbOwmspNf4Nz_Gd_9_Xt6nEig130_provenance.
- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion description "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_provenance.