Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_assertion description "[The motor neurons of patients with sporadic amyotrophic lateral sclerosis (ALS) express abundant Q/R site-unedited GluR2 mRNA, whereas those of patients with other motor neuron diseases including familial ALS associated with mutated SOD1 (ALS1) and those of normal subjects express only Q/R site-edited GluR2 mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_assertion evidence source_evidence_literature NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_assertion SIO_000772 20424386 NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_assertion wasDerivedFrom befree-20150227 NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_assertion wasGeneratedBy ECO_0000203 NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433781.RAnWA_SReu94Yt0_UPpQ8dI1HGzBnPWneV2DK2wuPr5tk130_provenance.