Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_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." NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_assertion evidence source_evidence_literature NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_assertion SIO_000772 25139356 NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_assertion wasDerivedFrom befree-20150227 NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_assertion wasGeneratedBy ECO_0000203 NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978606.RAHb2JEtg4nwpusu9gj0v4OStJ7cLgTX5PxDKRhFQVckQ130_provenance.