Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_assertion> ?p ?o ?g. }
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- NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_assertion type Assertion NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_head.
- NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_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." NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_provenance.
- NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_assertion evidence source_evidence_literature NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_provenance.
- NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_assertion SIO_000772 16683402 NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_provenance.
- NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_assertion wasDerivedFrom gad-20130706 NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_provenance.
- NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_assertion wasGeneratedBy ECO_0000203 NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ_Ls130_provenance.