Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_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." NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_assertion evidence source_evidence_literature NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_assertion SIO_000772 22683047 NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_assertion wasDerivedFrom befree-2016 NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_assertion wasGeneratedBy ECO_0000203 NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.
- befree-2016 importedOn "2016-02-19" NP988521.RAy6da_1mtPzqp5WEH5sAVFeIhc_6tMpF8tuCPANLCfhg130_provenance.