Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion> ?p ?o ?g. }
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- NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion type Assertion NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_head.
- NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion description "[In this study, we have applied 250K SNP array technology to detect previously cryptic chromosomal changes, particularly UPD, in a cohort of 301 patients with myelodysplastic syndromes (MDS), overlap MDS/myeloproliferative disorders (MPD), MPD, and acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_provenance.
- NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion evidence source_evidence_literature NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_provenance.
- NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion SIO_000772 19074904 NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_provenance.
- NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion wasDerivedFrom befree-20140225 NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_provenance.
- NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_assertion wasGeneratedBy ECO_0000203 NP409719.RAriCqzDJgY5dqoEcxQFZ0LKEF6s5I4Gc_EmNTHcTGZ7g130_provenance.