Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion> ?p ?o ?g. }
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- NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion type Assertion NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_head.
- NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion description "[In contrast to previous reports, homozygosity for the Asp298 variant of the 894G>T polymorphism in the eNOS gene was not found to be associated with risk of AMI, extent of CAD and in-hospital mortality after AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_provenance.
- NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion evidence source_evidence_literature NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_provenance.
- NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion SIO_000772 18495009 NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_provenance.
- NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion wasDerivedFrom gad-20150221 NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_provenance.
- NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_assertion wasGeneratedBy ECO_0000203 NP79796.RA_V3kYHs8gN_FESHbFcUZ7HwFqCFnUcwaYvZyJKTq3HU130_provenance.