Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- befree-2016 importedOn "2016-02-19" NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_assertion wasGeneratedBy ECO_0000203 NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_assertion wasDerivedFrom befree-2016 NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_assertion SIO_000772 10712198 NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_assertion evidence source_evidence_literature NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.
- NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_assertion description "[Using RED, we have identified a BPAD individual with a very large CAG/CTG repeat that is not due to expansion at SEF2-1B or ERDA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277683.RA6Ys3tAuspRMFPo3u5nUpu28pBApzwa3nxH_lHAeCz5A130_provenance.