Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_assertion description "[We have studied the influence of phosphorylation of human wild-type cTnI and of two mutant cTnI (G203S and K206Q) causing familial hypertrophic cardiomyopathy (fHCM) on the secondary structure by circular dichroism spectroscopy and on the Ca2+ regulation of actin-myosin interaction using actoS1-ATPase activity and in vitro motility assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_assertion evidence source_evidence_literature NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_assertion SIO_000772 14596793 NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_assertion wasDerivedFrom befree-20150227 NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_assertion wasGeneratedBy ECO_0000203 NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP356665.RA2Bjrc4R6CbKzalnCMBHUBG2j1cp41Ce9HxY3uyMFzB0130_provenance.