Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_assertion description "[This study shows that genetic variation of the AGT (M235T), but not the ACE (I/D), genotypes contributes to the presence of CHD independently of blood pressure profile in a subset of the Spanish population with a high prevalence of cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_assertion evidence source_evidence_literature NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_assertion SIO_000772 11345362 NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_assertion wasDerivedFrom befree-2016 NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_assertion wasGeneratedBy ECO_0000203 NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.
- befree-2016 importedOn "2016-02-19" NP317506.RAwAjYnZdhMKtaqF_Wf55fPC5w1fL0BNSjc8Kq2lbW0Dg130_provenance.