Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion> ?p ?o ?g. }
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- NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion type Assertion NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_head.
- NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion description "[We conclude that the 5q-syndrome may be best defined as primary MDS of the FAB type RA with a 5q deletion as the sole karyotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_provenance.
- NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion evidence source_evidence_literature NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_provenance.
- NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion SIO_000772 7604812 NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_provenance.
- NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion wasDerivedFrom befree-20150227 NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_provenance.
- NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_assertion wasGeneratedBy ECO_0000203 NP781564.RACLDbxnn3U1eS0v8sBk7S7YQEyk5Wl7uoL7rEBRLvqXk130_provenance.