Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP747886.RArDCA6l3GcjRh5S__n5UGsNpTvKBb15cu5nFYMQSqJyc130_provenance.