Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion> ?p ?o ?g. }
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- NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion type Assertion NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_head.
- NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion description "[Our findings identify TNFRSF14 as a candidate gene associated with a subset of FL, based on frequent occurrence of acquired mutations and their correlation with inferior clinical outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion evidence source_evidence_literature NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion SIO_000772 20884631 NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion wasDerivedFrom befree-20140225 NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_assertion wasGeneratedBy ECO_0000203 NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.