Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion> ?p ?o ?g. }
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- NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion type Assertion NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_head.
- NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion description "[In conclusion, the results of the present study provide evidence that C3435T MDR1 polymorphism may involve both the susceptibility to and the clinical outcome of childhood ALL. Carriers of the TT genotype are more at risk of developing ALL than other indi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_provenance.
- NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion evidence source_evidence_literature NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_provenance.
- NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion SIO_000772 15059065 NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_provenance.
- NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion wasDerivedFrom gad-20150221 NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_provenance.
- NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_assertion wasGeneratedBy ECO_0000203 NP61351.RAulAOyEYAFqM74wVSWZy7u6AdZhpClIM7n_FnmhUUOfA130_provenance.