Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion type Assertion NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_head.
- NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion description "[Variation in the VEGF gene is weakly associated with IMT and the risk of AMI, but the effect can only be observed when the information of the SNPs is combined by constructing haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_provenance.
- NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion evidence source_evidence_literature NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_provenance.
- NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion SIO_000772 19089753 NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_provenance.
- NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion wasDerivedFrom gad-20150221 NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_provenance.
- NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_assertion wasGeneratedBy ECO_0000203 NP86359.RAFLJsfP-we1VHvYwcOKFj0-4cKV9rxd31RFHTiYl0HcI130_provenance.