Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_assertion description "[This suggests that NMD may be detrimental for HDGC patients and therefore NMD is a potentially useful therapeutic target for CDH1 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_assertion evidence source_evidence_literature NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_assertion SIO_000772 18427545 NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_assertion wasDerivedFrom befree-2016 NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_assertion wasGeneratedBy ECO_0000203 NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.
- befree-2016 importedOn "2016-02-19" NP667149.RAjpHW8p4S3uiYnNk9eQaQtitFETzAajssesA__7CLIY0130_provenance.