Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_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." NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_assertion evidence source_evidence_literature NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_assertion SIO_000772 20424386 NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_assertion wasDerivedFrom befree-2016 NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_assertion wasGeneratedBy ECO_0000203 NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.
- befree-2016 importedOn "2016-02-19" NP808684.RAGiEfHCJmpOrwBmdv3MY8zssY_U6hOlrmGM1JxSbGK2E130_provenance.