Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_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." NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_assertion evidence source_evidence_literature NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_assertion SIO_000772 15551023 NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_assertion wasDerivedFrom befree-20140225 NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_assertion wasGeneratedBy ECO_0000203 NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP677685.RA9OoAG3s9DkHnRChThrSsGgPn3m55QSlee7k9veFHkRI130_provenance.