Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_assertion description "[In addition to new mutations in known SCD genes, several novel genes not previously implicated in SCD causation have been found, particularly in long QT syndrome (e.g., KCNJ5, AKAP9, SNTA1), idiopathic ventricular fibrillation (e.g., DPP6, KCNJ8), dilated cardiomyopathy (e.g., NEBL), and hypertrophic cardiomyopathy (HCM; e.g., NEXN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_assertion evidence source_evidence_literature NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_assertion SIO_000772 21430528 NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_assertion wasDerivedFrom befree-20150227 NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_assertion wasGeneratedBy ECO_0000203 NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP701896.RAV_twKn5-GMT7Wt_wVB9nRfjwu-KRlFyLnHABx7VwdJA130_provenance.