Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_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." NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_assertion evidence source_evidence_literature NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_assertion SIO_000772 20201937 NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_assertion wasDerivedFrom gad-20150221 NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_assertion wasGeneratedBy ECO_0000203 NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP166615.RAi_2cjvDy78RB7bHH7JGCejAejc2YDKglWAS7K5g0eu4130_provenance.