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- source_evidence_literature type ECO_0000212 NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_assertion description "[We studied the frequency of IgH (14q32) rearrangements and their partner chromosomes in 16 Japanese patients with MGUS (13 cases), and SMM (3 cases) by means of interphase double-color fluorescence in situ hybridization (DCFISH) applied to purified plasma cells and using CD138-bead selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_assertion evidence source_evidence_literature NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_assertion SIO_000772 12824903 NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_assertion wasDerivedFrom befree-20140225 NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_assertion wasGeneratedBy ECO_0000203 NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783409.RALyF5mZ9EcB_9vI0y8HvGz8SaEa0HGMjvZjTgrpxjo7g130_provenance.