Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP3023.RAdXcDVXct6Gvza_OTuC8ABFnPoRo-8ObFpGdUszHs9uM130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3023.RAdXcDVXct6Gvza_OTuC8ABFnPoRo-8ObFpGdUszHs9uM130_provenance.
• NP17891.RAizcSqvBp2OEYMajsaYCsFpSN5AHjsEFrMVKdy82TxzQ130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17891.RAizcSqvBp2OEYMajsaYCsFpSN5AHjsEFrMVKdy82TxzQ130_provenance.
• NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
• NP17007.RASYm7eDA4_V5OhkIHwZWeKT-PPNltCfu_kP2d1nH4DXc130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17007.RASYm7eDA4_V5OhkIHwZWeKT-PPNltCfu_kP2d1nH4DXc130_provenance.
• NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
• NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_provenance.
• NP450377.RAYyieD4nUq_Izj5mLV3PGvUYnbQfJwuE35bv_iUAObgQ130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450377.RAYyieD4nUq_Izj5mLV3PGvUYnbQfJwuE35bv_iUAObgQ130_provenance.
• assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
• NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_provenance.
• NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
• NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_provenance.
• NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
• NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_provenance.