Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_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." NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_assertion evidence source_evidence_literature NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_assertion SIO_000772 23575477 NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_assertion wasDerivedFrom befree-20150227 NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_assertion wasGeneratedBy ECO_0000203 NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP379646.RAWJ8C5sGcl_t6lGr3ufb6zZ3Wc0ezdf8VrcpQCd-fxnA130_provenance.