Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_assertion description "[ NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death. It is the second de novo mutation identified in NKX2.5. (2) NKX2.5 mutations are rare in sporadic CHD patients. (3) This study for the first time identifies association between]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_assertion evidence source_evidence_literature NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_assertion SIO_000772 20932824 NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_assertion wasDerivedFrom gad-20150221 NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_assertion wasGeneratedBy ECO_0000203 NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.