Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion> ?p ?o ?g. }
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- NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion type Assertion NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_head.
- NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion description "[ADA deficiency in at least two mutant cell lines is not caused by deficient levels of translatable mRNA, and unless there is some translational control of this mRNA, the characteristic cellular ADA deficiency is most likely secondary to synthesis and rapid degradation of a defective ADA protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion evidence source_evidence_literature NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion SIO_000772 6134754 NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion wasDerivedFrom befree-2016 NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion wasGeneratedBy ECO_0000203 NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.