Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_assertion description "[Recently, various human studies have revealed a high coincidence of VEGF and NOTCH polymorphisms with cardiovascular outflow tract anomalies, such as bicuspid aortic valves and Tetralogy of Fallot, next to predisposition for cardiovascular pathologies, including atherosclerosis and aortic valve calcification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_assertion evidence source_evidence_literature NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_assertion SIO_000772 22683047 NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_assertion wasDerivedFrom befree-20150227 NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_assertion wasGeneratedBy ECO_0000203 NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP771146.RAXUOiqhjlhx2LIiDxh9Q_w7i9rF7O9UMciprdXiDK0qc130_provenance.