Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_assertion evidence source_evidence_literature NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_assertion SIO_000772 24684794 NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_assertion wasDerivedFrom befree-2016 NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_assertion wasGeneratedBy ECO_0000203 NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1168892.RAkijvR-BMLC8f7bUtBqBP8LzaL44aYNi3dN-gG6otFf4130_provenance.