Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_assertion description "[Multivariate analyses to examine the joint effects of multiple gene variants confirmed univariate results for MYH7 and TCAP and identified a block of nine variants in MYH7 that was strongly associated with DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_assertion evidence source_evidence_literature NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_assertion SIO_000772 20201937 NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_assertion wasDerivedFrom befree-2016 NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_assertion wasGeneratedBy ECO_0000203 NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP797700.RAPe9eGfi_WsZlXanry5s1iMy6HxFw71R7OrCXxJg1JiQ130_provenance.