Matches in Nanopublications for { ?s ?p "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP621506.RArQXNBLJtzAcqEFwgMDPAVvZfVYEh6KbZcczhybwygN4130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621506.RArQXNBLJtzAcqEFwgMDPAVvZfVYEh6KbZcczhybwygN4130_provenance.
- NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- NP604068.RA-AGU1ktRbWPLFxarFQ8eq9y6hXYCNzx8XWXB_wwdqAk130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604068.RA-AGU1ktRbWPLFxarFQ8eq9y6hXYCNzx8XWXB_wwdqAk130_provenance.
- NP361175.RASo_zDaR9lQlCwhmyMonUBGnx4RNOt3LvZqEDdEjeQdc130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361175.RASo_zDaR9lQlCwhmyMonUBGnx4RNOt3LvZqEDdEjeQdc130_provenance.
- assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- NP316519.RAgYRlH08y4qSYE432BZPwue7dDnc6JcurhhSEgArOO0s130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316519.RAgYRlH08y4qSYE432BZPwue7dDnc6JcurhhSEgArOO0s130_provenance.