Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_assertion description "[The purpose of this study was to determine whether the deletion/insertion (D/I) polymorphism in the ACE-encoded angiotensin-converting enzyme or the pooled gene effect of five renin-angiotensin-aldosterone system (RAAS) polymorphisms were disease modifiers in a large cohort of unrelated patients with genotyped hypertrophic cardiomyopathy (HCM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_assertion evidence source_evidence_literature NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_assertion SIO_000772 16087648 NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_assertion wasDerivedFrom gad-20130706 NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_assertion wasGeneratedBy ECO_0000203 NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49500.RA36cDGoeD8kM2Wz2hnsVjkz0aE2tVQr4NyDBA0tJb3Vo130_provenance.