Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_assertion wasGeneratedBy ECO_0000203 NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_assertion wasDerivedFrom lhgdn-20090331 NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_assertion SIO_000772 18413471 NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_assertion evidence source_evidence_literature NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.
- NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_assertion description "[No large deletions at the SCN1A locus were found in any of the patients/different point mutations were identified in 12 patients: 10 with SMEI, 1 with generalized epilepsy with febrile seizures plus, and 1 with cryptogenic focal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236727.RA1bUEKf6Z3CxvEewf2pYQXYnO2C3fc36eiUoURrsShIA130_provenance.