Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.
- 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.
- gad-20130706 importedOn "2013-07-06" NP77634.RANo8CacFwbwI4nNTpJ85lci-5BCG21_-nOVNpQbBuRAY130_provenance.