Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP261655.RACJRJEbamRz-sqdbKol3XOQoKTzS8ZTQkFBprNUXeUXk130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261655.RACJRJEbamRz-sqdbKol3XOQoKTzS8ZTQkFBprNUXeUXk130_provenance.
• NP359892.RAA6Hwd3TKwCBdk2GhqnMh-3my_CaqGaDVm6JF_FWh00o130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359892.RAA6Hwd3TKwCBdk2GhqnMh-3my_CaqGaDVm6JF_FWh00o130_provenance.
• NP174930.RAZ7z7v_9hLhTzOahX8kTWrlYP3OL7fnvPb24Ge85JUZk130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174930.RAZ7z7v_9hLhTzOahX8kTWrlYP3OL7fnvPb24Ge85JUZk130_provenance.
• NP259950.RAsX0fGSNgsbSkniN-pQMvynPBoCj9KhutMipgal3kBkE130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259950.RAsX0fGSNgsbSkniN-pQMvynPBoCj9KhutMipgal3kBkE130_provenance.
• NP312768.RAsDLuabJKg0rZyF5ynZ5ZIXpaAhkL-r8yUpw4BYrQNL4130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312768.RAsDLuabJKg0rZyF5ynZ5ZIXpaAhkL-r8yUpw4BYrQNL4130_provenance.
• NP388548.RAqxiI_GaN4ak7UHfcNFtzLtHU1YmmvUQ2SlzigHtKccI130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388548.RAqxiI_GaN4ak7UHfcNFtzLtHU1YmmvUQ2SlzigHtKccI130_provenance.
• NP534643.RA6hCkdTDto-p9cq9ijS9Ndz5fImE0ShAfxefaW08uakA130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534643.RA6hCkdTDto-p9cq9ijS9Ndz5fImE0ShAfxefaW08uakA130_provenance.
• NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
• NP782587.RAfzFxhn37Y2MpLnz0qwnoF02xgb7wnaHNFz3Rrqldp2I130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782587.RAfzFxhn37Y2MpLnz0qwnoF02xgb7wnaHNFz3Rrqldp2I130_provenance.
• assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP408695.RAWrimaGfWHgVodIKTYQiGrgBIYo7AkfeSXW5ipjkH8m4130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408695.RAWrimaGfWHgVodIKTYQiGrgBIYo7AkfeSXW5ipjkH8m4130_provenance.
• NP408692.RAvhAXulwERbhO6yFaZnzdIrY5yjH2UzGG5NUf1LJzJyU130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408692.RAvhAXulwERbhO6yFaZnzdIrY5yjH2UzGG5NUf1LJzJyU130_provenance.
• NP408691.RAz22oAEXUu23nc8Mjrq6BJPW2qc6-e_-gyTAItVIqf7g130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408691.RAz22oAEXUu23nc8Mjrq6BJPW2qc6-e_-gyTAItVIqf7g130_provenance.