Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_assertion description "[Subset analysis of the two most common genetic subtypes of HCM, MYBPC3 (myosin binding protein C) and MYH7 (beta myosin heavy chain), demonstrated a significant pro-LVH effect of DD-ACE only in patients with MYBPC3-HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_assertion evidence source_evidence_literature NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_assertion SIO_000772 16087648 NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_assertion wasDerivedFrom befree-2016 NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_assertion wasGeneratedBy ECO_0000203 NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.
- befree-2016 importedOn "2016-02-19" NP507992.RAH05vapNL3SMOnjFOi3r_p1lUDpn1RpYtxnvcLqifwgA130_provenance.