Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_assertion description "[Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_assertion evidence source_evidence_literature NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_assertion SIO_000772 17334235 NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_assertion wasDerivedFrom befree-2016 NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_assertion wasGeneratedBy ECO_0000203 NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.
- befree-2016 importedOn "2016-02-19" NP596871.RACPfPVZT6bsl76Ry5sGExiA5lfmaQVhYDSQ_OTPTsaQg130_provenance.