Matches in Nanopublications for { ?s ?p "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP527154.RAWJC7aMPP49h7BvGEQnIa_gm_zKhUebdYU6gm1MBZ6aU130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527154.RAWJC7aMPP49h7BvGEQnIa_gm_zKhUebdYU6gm1MBZ6aU130_provenance.
- NP448132.RAnDYeS0FsMt_SpDdL6ov4BRNGrluc1T3dcudEYy-E_sc130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448132.RAnDYeS0FsMt_SpDdL6ov4BRNGrluc1T3dcudEYy-E_sc130_provenance.
- NP840974.RAm_iLdMbD1m0-JXmZ3NxIdN1KJhqexKZAHQe1rU2ZPmI130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840974.RAm_iLdMbD1m0-JXmZ3NxIdN1KJhqexKZAHQe1rU2ZPmI130_provenance.
- assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_provenance.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_provenance.
- NP463782.RANX5lT_I614JVPNmA9O6lgSy4hZaEmxETJXqfEQyhh3c130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463782.RANX5lT_I614JVPNmA9O6lgSy4hZaEmxETJXqfEQyhh3c130_provenance.
- NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- NP854122.RAOjvKe7iDAWsGYxqq6IDSluTdtiYxu2ICTrJ9N0jgw_Y130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854122.RAOjvKe7iDAWsGYxqq6IDSluTdtiYxu2ICTrJ9N0jgw_Y130_provenance.