Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_assertion description "[In this study, we determined the PCLI and the deletion of 13q14, retinoblastoma-1 gene (RB-1), 1p13, and 17p13, 1q21 amplification, and IgH rearrangements in 42 newly diagnosed patients with MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_assertion evidence source_evidence_literature NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_assertion SIO_000772 21133734 NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_assertion wasDerivedFrom befree-2016 NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_assertion wasGeneratedBy ECO_0000203 NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.
- befree-2016 importedOn "2016-02-19" NP857134.RAnGZz5ydTcecoYqJFWrys7MeZRE8BA5CKkgW7nuV65Ls130_provenance.