Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_assertion description "[Somatic mutations in AA patients with a disease duration of >6 months were associated with a 40% risk of transformation to MDS (P < .0002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_assertion evidence source_evidence_literature NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_assertion SIO_000772 25139356 NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_assertion wasDerivedFrom befree-20150227 NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_assertion wasGeneratedBy ECO_0000203 NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781516.RADbcCtJYpThF-4LK80EQN9F6IWcH6md1OC1S1DHmvAcU130_provenance.