Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion> ?p ?o ?g. }
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- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion type Assertion NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_head.
- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion wasGeneratedBy ECO_0000203 NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_provenance.
- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion wasDerivedFrom gad-20150221 NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_provenance.
- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion SIO_000772 16298355 NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_provenance.
- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion evidence source_evidence_literature NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_provenance.
- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_provenance.