Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion description "[It is worthwhile to point out that such a highly polymorphic DNA sequence is located in the same chromosomal region where so much somatic rearrangement goes on normally (i.e., switch region between classes of heavy chain constant region genes) and which is involved with de novo translocations associated with malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion evidence source_evidence_literature NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion SIO_000772 6818543 NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion wasDerivedFrom befree-20140225 NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion wasGeneratedBy ECO_0000203 NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance.