Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_assertion description "[Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_assertion evidence source_evidence_literature NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_assertion SIO_000772 18006695 NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_assertion wasDerivedFrom gad-20150221 NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_assertion wasGeneratedBy ECO_0000203 NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP115231.RAmHr3h2J1eXwEe9nP19AKu2FqwO1s1w8QYCWptG30wK0130_provenance.