Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion type Assertion NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_head.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_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." NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_provenance.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion evidence source_evidence_literature NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_provenance.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion SIO_000772 20137776 NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_provenance.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion wasDerivedFrom befree-2016 NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_provenance.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion wasGeneratedBy ECO_0000203 NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_provenance.