Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion> ?p ?o ?g. }
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- NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion type Assertion NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_head.
- NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion wasGeneratedBy ECO_0000203 NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_provenance.
- NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion wasDerivedFrom gad-20150221 NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_provenance.
- NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion SIO_000772 20586826 NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_provenance.
- NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion evidence source_evidence_literature NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_provenance.
- NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_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." NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_provenance.