Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_assertion description "[Comprehensive genomic profiling of relapsed CDH1-mutated ILC revealed actionable genomic alterations in 86% of cases, featured a high incidence of ERBB2 alterations, and can reveal actionable alterations that can inform treatment decisions for patients with ILC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_assertion evidence source_evidence_literature NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_assertion SIO_000772 23575477 NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_assertion wasDerivedFrom befree-20140225 NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_assertion wasGeneratedBy ECO_0000203 NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP593787.RAPgFTBycSCEDskeHMaJTkMIhfrX4Z6QQ0n7ZiZfMuH_s130_provenance.