Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_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." NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_assertion evidence source_evidence_literature NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_assertion SIO_000772 22972638 NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_assertion wasDerivedFrom befree-20140225 NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_assertion wasGeneratedBy ECO_0000203 NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435296.RA3D5ptdpzYmt0helYre4-9VNDHUIei2nwUnqvA-mjmi4130_provenance.