Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion> ?p ?o ?g. }
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- NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion type Assertion NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_head.
- NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion description "[Analysis for loss of heterozygosity on chromosome arm 13q by STR analysis or SNP sequencing can replace analysis of FLT3-ITD to detect patients with prognostically adverse AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_provenance.
- NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion evidence source_evidence_literature NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_provenance.
- NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion SIO_000772 25183446 NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_provenance.
- NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion wasDerivedFrom befree-2016 NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_provenance.
- NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_assertion wasGeneratedBy ECO_0000203 NP1216381.RA89esyjBc41lk1H4DJimZplzHUQDaNPNhUmCsd5zxVQc130_provenance.