Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion> ?p ?o ?g. }
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- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion type Assertion NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_head.
- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion description "[We performed mutational analysis of MNX1 in all cases by DNA sequencing as well as by Multiplex Ligation-dependent Probe Amplification (MLPA) in those CS cases where no MNX1 mutations were found, to exclude a MNX1 heterozygous loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_provenance.
- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion evidence source_evidence_literature NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_provenance.
- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion SIO_000772 24095820 NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_provenance.
- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion wasDerivedFrom befree-2016 NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_provenance.
- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion wasGeneratedBy ECO_0000203 NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_provenance.