Matches in Nanopublications for { ?s ?p "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_provenance.
- NP350637.RAeYf3DTDM6uUCx_3OHW7W2u7zwp-UajVkP5id2uY1EFQ130_assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350637.RAeYf3DTDM6uUCx_3OHW7W2u7zwp-UajVkP5id2uY1EFQ130_provenance.
- NP1137368.RAfKcLo7ueQ7UMY9hXYpQ_ISu9LkK38TWghFfQ2kjYk4U130_assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1137368.RAfKcLo7ueQ7UMY9hXYpQ_ISu9LkK38TWghFfQ2kjYk4U130_provenance.
- NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1137369.RAas4JHYKeoSFkr6ysnlDPGtyTLOtcgSLg7q0HMPgelDM130_provenance.