Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_assertion description "[Results were similar when the analysis was restricted to MDS and CMML patients, excluding AML (HR=2.46 (95% confidence interval: 1.1-6.4); p=0.04)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_assertion evidence source_evidence_literature NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_assertion SIO_000772 24836762 NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_assertion wasDerivedFrom befree-2016 NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_assertion wasGeneratedBy ECO_0000203 NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1183168.RAugrIpCU9rAzNDz0Fk2B9GuYytgCN6SRnj-hQAqpiv5g130_provenance.