Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance.