Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_assertion description "[Subsequent sequence and genotype analysis identified EIF4G1 c.1505C>T (p.Ala502Val), c.2056G>T (p.Gly686Cys), c.3490A>C (p.Ser1164Arg), c.3589C>T (p.Arg1197Trp) and c.3614G>A (p.Arg1205His) substitutions in affected subjects with familial parkinsonism and idiopathic Lewy body disease but not in control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_assertion evidence source_evidence_literature NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_assertion SIO_000772 21907011 NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_assertion wasDerivedFrom befree-20150227 NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_assertion wasGeneratedBy ECO_0000203 NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP372438.RAb_rvnOef7w-CNrWY_BjOTq_-R6euttSxa3lzfKZoue4130_provenance.