Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion> ?p ?o ?g. }
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- NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion type Assertion NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_head.
- NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion description "[In the alveolar subtype, 2 recurrent chromosomal translocations, t(2;13)(q35;q14) and its variant t(1;13)(p36;q14), have been identified as the specific cytogenetic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_provenance.
- NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion evidence source_evidence_literature NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_provenance.
- NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion SIO_000772 19215790 NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_provenance.
- NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion wasDerivedFrom befree-20140225 NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_provenance.
- NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_assertion wasGeneratedBy ECO_0000203 NP159365.RACxG990NYwozRPas_xTZzjPQ7G_X0imX6sT0NdfKWGnM130_provenance.