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- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion type Assertion NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_head.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion description "[The common aberration found in these two t-MDS cases was the fragility of chromosome 5 and monosomy of chromosome 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion evidence source_evidence_literature NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion SIO_000772 12505257 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion wasDerivedFrom befree-20150227 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion wasGeneratedBy ECO_0000203 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.