Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion> ?p ?o ?g. }
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- NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion type Assertion NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_head.
- NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion wasGeneratedBy ECO_0000203 NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_provenance.
- NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion wasDerivedFrom gad-20150221 NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_provenance.
- NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion SIO_000772 20586826 NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_provenance.
- NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion evidence source_evidence_literature NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_provenance.
- NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_provenance.