Matches in Nanopublications for { ?s ?p "[The proximal myotonic myopathy phenotype is associated with DM2- (CCTG) (n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP153608.RAoxt3GelDMSmLvX-HcfJ_oa3H0coKiHZ0G764Fj-YKo8130_assertion description "[The proximal myotonic myopathy phenotype is associated with DM2- (CCTG) (n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153608.RAoxt3GelDMSmLvX-HcfJ_oa3H0coKiHZ0G764Fj-YKo8130_provenance.
- assertion description "[The proximal myotonic myopathy phenotype is associated with DM2- (CCTG) (n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP216715.RAgeay-XkZgU-Gs81IQz1gA6YzN1w5hfsnzoa0v9hrv7c130_assertion description "[The proximal myotonic myopathy phenotype is associated with DM2- (CCTG) (n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216715.RAgeay-XkZgU-Gs81IQz1gA6YzN1w5hfsnzoa0v9hrv7c130_provenance.
- NP205996.RAim3aePGRWPTMbs1ZRKShH722Q7uUZfpDqxK8O0O0PXk130_assertion description "[The proximal myotonic myopathy phenotype is associated with DM2- (CCTG) (n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205996.RAim3aePGRWPTMbs1ZRKShH722Q7uUZfpDqxK8O0O0PXk130_provenance.