Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_assertion description "[This meta-analysis suggests that cardiomyopathy due to lamin A/C gene mutations portends a high risk of sudden death, and that this risk does not differ between subjects with predominantly cardiac or neuromuscular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_assertion evidence source_evidence_literature NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_assertion SIO_000772 15551023 NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_assertion wasDerivedFrom befree-20150227 NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_assertion wasGeneratedBy ECO_0000203 NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537509.RAbKc8Zi4FrTYhhu4mHM1L3alUpVVTno_RLMLwVgwNEoM130_provenance.