Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion> ?p ?o ?g. }
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- NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion type Assertion NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_head.
- NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion description "[To examine the association of genetic polymorphisms in this region with chronic kidney disease (CKD; estimated glomerular filtration rate <60 ml/min/1.73 m(2)) in individuals of European ancestry, we examined rs4821480, an MYH9 single-nucleotide polymorphism (SNP) recently identified as associated with kidney disease in African-Americans, in 13 133 participants from the Framingham Heart Study (FHS) and Atherosclerosis Risk in Communities (ARIC) Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_provenance.
- NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion evidence source_evidence_literature NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_provenance.
- NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion SIO_000772 21429915 NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_provenance.
- NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion wasDerivedFrom befree-20150227 NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_provenance.
- NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_assertion wasGeneratedBy ECO_0000203 NP583453.RA3nr1asBrrwDa4fN7MhiKsejXRVl-W6V4XlQr2P4hf1U130_provenance.