Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP678479.RAWb7mWk-YSi3GfuNlpNCFpmGPgvBZ3IZl2gobLDgn6Kg130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678479.RAWb7mWk-YSi3GfuNlpNCFpmGPgvBZ3IZl2gobLDgn6Kg130_provenance.
• NP196816.RAuh6UR0G3_wItx1e4shvvr2S8uQHip3Iyb3df6VVaKIs130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196816.RAuh6UR0G3_wItx1e4shvvr2S8uQHip3Iyb3df6VVaKIs130_provenance.
• NP282858.RAkbvqL7Td2BTF691PtIOBF0cD6gxFtmsslKomdIumfus130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282858.RAkbvqL7Td2BTF691PtIOBF0cD6gxFtmsslKomdIumfus130_provenance.
• NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_provenance.
• NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_provenance.
• NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_provenance.
• NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
• NP329155.RA_ugME_bZXYPF0jy_4-WzthIxoZT3BfWIiXqyqNxNuHs130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329155.RA_ugME_bZXYPF0jy_4-WzthIxoZT3BfWIiXqyqNxNuHs130_provenance.
• NP329158.RA_cizzZTPlxy8Mv-3TNvXXZAXTZr6xL0ikZ72VdWtF08130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329158.RA_cizzZTPlxy8Mv-3TNvXXZAXTZr6xL0ikZ72VdWtF08130_provenance.
• NP329148.RAXb0SrvP6ZRqQAaeZEFzInEha0OhdS5cNjjNVXI665Lw130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329148.RAXb0SrvP6ZRqQAaeZEFzInEha0OhdS5cNjjNVXI665Lw130_provenance.
• NP329150.RAdOHE6c0dvbkTHxD09oqnOIJpy_qXY34KB2zTMiaSGzE130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329150.RAdOHE6c0dvbkTHxD09oqnOIJpy_qXY34KB2zTMiaSGzE130_provenance.
• assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP329154.RAObKpH3PSIfe22hSUuSt7QpMo_xs8N8DNsFyrH499uTw130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329154.RAObKpH3PSIfe22hSUuSt7QpMo_xs8N8DNsFyrH499uTw130_provenance.
• NP662212.RApmVZlyklS4xl4JT9ynViMeO2qsSsUionmY2qVZIOklo130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662212.RApmVZlyklS4xl4JT9ynViMeO2qsSsUionmY2qVZIOklo130_provenance.