Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_assertion description "[A GCG trinucleotide expansion (GCG)10+7 and a deletion of 1,517 bp in the ARX gene have also been found in association with the West syndrome, and a missense mutation (1058C>T) in a family with a newly recognized form of myoclonic epilepsy, severe mental retardation, and spastic paraplegia [Scheffer et al., 2002: Neurology, in press].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_assertion evidence source_evidence_literature NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_assertion SIO_000772 12376946 NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_assertion wasDerivedFrom befree-2016 NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_assertion wasGeneratedBy ECO_0000203 NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.
- befree-2016 importedOn "2016-02-19" NP370835.RAP54HCDFGGt3H8wNqp8DZdczPeBW2owJ5A9Z8lfbpstY130_provenance.