Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_assertion> ?p ?o ?g. }
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- NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_assertion SIO_000772 24684794 NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_provenance.
- NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_assertion evidence source_evidence_literature NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_provenance.
- NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_assertion description "[Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_provenance.