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Matches in Nanopublications for { ?s ?p "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_provenance.
• assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1168895.RAVmSNiIZ8-wo79ElBI-0QSiyzEN4j8dneAwHUOcJYnOU130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168895.RAVmSNiIZ8-wo79ElBI-0QSiyzEN4j8dneAwHUOcJYnOU130_provenance.
• NP706673.RAlo3zDewP17aQdqseqdd_hi5aJ65YOZBZEfgdvVpIgWo130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706673.RAlo3zDewP17aQdqseqdd_hi5aJ65YOZBZEfgdvVpIgWo130_provenance.
• NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895447.RACcMJWQ_ogB-AL-EPbrh-ItLuSh8U0Sp2SGrP7y55Hqc130_provenance.
• NP484520.RAmpRlQkkr4hWURCpgzlxl3hBRDn_08P77wP4odVyc9sg130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484520.RAmpRlQkkr4hWURCpgzlxl3hBRDn_08P77wP4odVyc9sg130_provenance.
• NP1168890.RAoUGGEvhUhn_I0vi4KX2K_k5Cla1ue31j024PZF5n4C4130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168890.RAoUGGEvhUhn_I0vi4KX2K_k5Cla1ue31j024PZF5n4C4130_provenance.
• NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
• NP1168894.RAvpzr_Xm1dQ5DrAP_8ntk2TWZI1fy84qfBp_w6rYFZNQ130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168894.RAvpzr_Xm1dQ5DrAP_8ntk2TWZI1fy84qfBp_w6rYFZNQ130_provenance.
• NP840242.RANQTX6_iT4lM0P6ltPzdi6m3-rM4xuLsF9vAeQzY0IxQ130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840242.RANQTX6_iT4lM0P6ltPzdi6m3-rM4xuLsF9vAeQzY0IxQ130_provenance.
• NP1168891.RAPiQ2tgf1I1E3hTGbBLI58YH_lvc729gd2EcOEQvYrYo130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168891.RAPiQ2tgf1I1E3hTGbBLI58YH_lvc729gd2EcOEQvYrYo130_provenance.
• NP706408.RA1IRaT0BfkNruCKyxLKJJkr1-wcSv5rMXe8dJdq3QLYY130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706408.RA1IRaT0BfkNruCKyxLKJJkr1-wcSv5rMXe8dJdq3QLYY130_provenance.
• NP1168893.RA3DPHDBLCykNxiu3Y6VMReehRH6ZYcl89DMyCqqthVms130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168893.RA3DPHDBLCykNxiu3Y6VMReehRH6ZYcl89DMyCqqthVms130_provenance.