Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion type Assertion NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_head.
- NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion wasGeneratedBy ECO_0000203 NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_provenance.
- NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion wasDerivedFrom lhgdn-20090331 NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_provenance.
- NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion SIO_000772 17512363 NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_provenance.
- NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion evidence source_evidence_literature NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_provenance.
- NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_assertion description "[multiple, less common SNPs and haplotype variants underlie CETP-related coronary artery disease risk; occurrence of risk-related variants on separate haplotypes suggests genetic-risk complexity and allelic heterogeneity]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197145.RAXdQDgXIribnmP69z6TxH5y03tkA4zZ0xjmLDr0tpjTg130_provenance.