Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- befree-2016 importedOn "2016-02-19" NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_assertion wasGeneratedBy ECO_0000203 NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_assertion wasDerivedFrom befree-2016 NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_assertion SIO_000772 16875940 NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_assertion evidence source_evidence_literature NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.
- NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_assertion description "[We propose that the del(20q) may have different clinical significance in plasma cell dyscrasia: one is when del(20q) appears at diagnosis and may involve the initial event of oncogenesis, and the other is when del(20q) appears after treatment and is associated with therapy-related and potential MDS/AML risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561893.RAgKoyuVnuMiY4RQMhnMF8LoBmaVmu9O8zj_SrXuljYhA130_provenance.