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- source_evidence_literature type ECO_0000212 NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_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." NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_assertion evidence source_evidence_literature NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_assertion SIO_000772 21430528 NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_assertion wasDerivedFrom befree-20150227 NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_assertion wasGeneratedBy ECO_0000203 NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP358744.RAFLwJuQO4VoQYYHNbLwWhCrk8p33Qr4hXajYibzAvsUs130_provenance.