Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
• NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
• NP704502.RA9aAeGQEoUK38JXiTLt2Yeiuwp-Cqq22c4TbLAu6FGCI130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704502.RA9aAeGQEoUK38JXiTLt2Yeiuwp-Cqq22c4TbLAu6FGCI130_provenance.
• assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP557504.RAJlCH4aggvtCnw0_7Zb_O27VBAeKp2VADyFJ7B8ZaYdc130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557504.RAJlCH4aggvtCnw0_7Zb_O27VBAeKp2VADyFJ7B8ZaYdc130_provenance.
• NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
• NP1376552.RANVmrmEH2Bewe1DD09f_9xT9JZvOgzWohAV96z75nuT8130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376552.RANVmrmEH2Bewe1DD09f_9xT9JZvOgzWohAV96z75nuT8130_provenance.
• NP1376551.RA1XlwZWwMNJSwnqgpQlkTIwo0b2iDTtlYO_VyJIDKu2A130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376551.RA1XlwZWwMNJSwnqgpQlkTIwo0b2iDTtlYO_VyJIDKu2A130_provenance.
• NP1376553.RAzAz-9FVuz5UNluIDf66fqy755HisNjKGb1Wp-1TBS4o130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376553.RAzAz-9FVuz5UNluIDf66fqy755HisNjKGb1Wp-1TBS4o130_provenance.