Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion> ?p ?o ?g. }
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- NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion type Assertion NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_head.
- NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_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." NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_provenance.
- NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion evidence source_evidence_literature NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_provenance.
- NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion SIO_000772 20586826 NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_provenance.
- NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion wasDerivedFrom gad-20150221 NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_provenance.
- NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion wasGeneratedBy ECO_0000203 NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_provenance.