Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_assertion wasGeneratedBy ECO_0000203 NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_assertion wasDerivedFrom befree-20150227 NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_assertion SIO_000772 11857753 NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_assertion evidence source_evidence_literature NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.
- NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_assertion description "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.