Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion> ?p ?o ?g. }
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- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion type Assertion NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_head.
- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion description "[Based on previous reports the frequency of co-segregating recessive chloride channel (CLCN1) mutations in families with myotonic dystrophy type 2 (DM2) was suspected to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion evidence source_evidence_literature NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion SIO_000772 18807109 NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion wasDerivedFrom gad-20130706 NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_assertion wasGeneratedBy ECO_0000203 NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.