Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_assertion description "[The polymorphism of Glu298Asp eNOS gene in dead cases may be useful for determining the cause of death in CHD cases in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_assertion evidence source_evidence_literature NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_assertion SIO_000772 16683402 NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_assertion wasDerivedFrom gad-20130706 NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_assertion wasGeneratedBy ECO_0000203 NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP61832.RAEFFydDBVwEKIlGxHdROah0o6ussJhWyyD4bNp7gpkbM130_provenance.