Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion> ?p ?o ?g. }
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- NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion type Assertion NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_head.
- NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion description "[We have demonstrated that the MTRR c.56+781 A>C variant is an important genetic marker for increased CHD risk because this variant results in functionally reduced MTRR expression at the transcriptional level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_provenance.
- NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion evidence source_evidence_literature NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_provenance.
- NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion SIO_000772 22179537 NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_provenance.
- NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion wasDerivedFrom befree-20140225 NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_provenance.
- NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_assertion wasGeneratedBy ECO_0000203 NP394069.RAIcAUWaS9NSgBIV5_gW0MzSQsu8eM0BKNTqUYOM3bsWc130_provenance.