Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_assertion description "[The MEF2A mutations may account for up to 1.93% of the disease population; thus, genetic testing based on mutational analysis of MEF2A may soon be available for many coronary artery disease/myocardial infarction patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_assertion evidence source_evidence_literature NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_assertion SIO_000772 15861005 NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_assertion wasDerivedFrom lhgdn-20090331 NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_assertion wasGeneratedBy ECO_0000203 NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP197307.RA79oh42rf6hpINcx7-W86UwRwKkn1AnCQRcbQGUyUiRU130_provenance.