Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion> ?p ?o ?g. }
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- NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion type Assertion NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_head.
- NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion description "[In addition, we suggest that der(17)t(12;17)(q13;p13) should be considered a new recurrent, nonrandom chromosomal abnormality in patients with t-MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_provenance.
- NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion evidence source_evidence_literature NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_provenance.
- NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion SIO_000772 19155067 NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_provenance.
- NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion wasDerivedFrom befree-2016 NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_provenance.
- NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_assertion wasGeneratedBy ECO_0000203 NP715435.RAsGDVdQOYnMel22Sp89VNDZGjg0soIX0pdO7NsVmr0Kw130_provenance.