Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion> ?p ?o ?g. }
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- NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion type Assertion NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_head.
- NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion description "[The K allele was significantly more frequent in FH subjects without premature CHD than in FH subjects with premature CHD suggesting that the genetic variant R219K in ABCA1 could influence the development and progression of atherosclerosis in FH subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_provenance.
- NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion evidence source_evidence_literature NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_provenance.
- NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion SIO_000772 12624133 NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_provenance.
- NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion wasDerivedFrom lhgdn-20090331 NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_provenance.
- NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_assertion wasGeneratedBy ECO_0000203 NP130038.RA1oSHAWIFfxEcXMlumQsMxRV-QNdw8MbUn5Sls-e7k4s130_provenance.