Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_assertion description "[Recurrent mutations in three main genes (SCN1A, SCN1B and GABRG2) have been identified that cause febrile seizures with or without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_assertion evidence source_evidence_literature NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_assertion SIO_000772 25362483 NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_assertion wasDerivedFrom befree-20150227 NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_assertion wasGeneratedBy ECO_0000203 NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682375.RAN8dKoinn1o2O_4K5FAOa0SJNqUMx9RyL0fRNN43NF8M130_provenance.