Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_assertion description "[Furthermore, 7 novel noncoding SQSTM1 variants were found in patients with FTLD and patients with ALS, including 4 variations in the promoter region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_assertion evidence source_evidence_literature NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_assertion SIO_000772 22972638 NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_assertion wasDerivedFrom befree-20140225 NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_assertion wasGeneratedBy ECO_0000203 NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213885.RA4BksNM3dtjnkj7xsDPF2EVhp7MZPrK0PmTJzuoGUfMU130_provenance.