Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_assertion> ?p ?o ?g. }
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- NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_assertion type Assertion NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_head.
- NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_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." NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_provenance.
- NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_assertion evidence source_evidence_literature NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_provenance.
- NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_assertion SIO_000772 15059065 NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_provenance.
- NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_assertion wasDerivedFrom gad-20150221 NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_provenance.
- NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_assertion wasGeneratedBy ECO_0000203 NP84665.RAF8k61ra4pmmY0o7r2mDZdE5eZwu6lnb_hxwQePSpJ3Y130_provenance.