Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_assertion description "[Hypertrophic cardiomyopathy is due to sarcomeric gene mutations, however, phenocopies with myocardial hypertrophy can be due to triplet-repeat syndromes (Friedreich ataxia and myotonic dystrophy), mitochondrial and metabolic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_assertion evidence source_evidence_literature NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_assertion SIO_000772 14711353 NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_assertion wasDerivedFrom befree-20150227 NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_assertion wasGeneratedBy ECO_0000203 NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411460.RAf3XUL-gu0R69nXJL1rYjT4OpRFtA4njHDlx7uKGAqBI130_provenance.