Matches in Nanopublications for { ?s ?p "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- assertion description "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP4.RAMnUqGlrpHndEURx4agoiLNLdG90GNF45fY8wxEcKf8E130_assertion description "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4.RAMnUqGlrpHndEURx4agoiLNLdG90GNF45fY8wxEcKf8E130_provenance.
- NP218011.RAXlehTQr8V9MVE6q4eTMMW_mkwb6PiOvHEQElZRissj8130_assertion description "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218011.RAXlehTQr8V9MVE6q4eTMMW_mkwb6PiOvHEQElZRissj8130_provenance.
- NP2722.RA1om4Dw8HQFVP5gAI0CjQcUK82_ThT5p6N-E_2XRSDT8130_assertion description "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2722.RA1om4Dw8HQFVP5gAI0CjQcUK82_ThT5p6N-E_2XRSDT8130_provenance.
- NP931985.RA8f4j9cwRV9kFM2VYJFEy1sY5FxNqGBN_WTnniY0vzuo130_assertion description "[A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931985.RA8f4j9cwRV9kFM2VYJFEy1sY5FxNqGBN_WTnniY0vzuo130_provenance.