Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion> ?p ?o ?g. }
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- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion type Assertion NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_head.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion evidence source_evidence_literature NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion SIO_000772 20137776 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion wasDerivedFrom befree-20140225 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion wasGeneratedBy ECO_0000203 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.