Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion type Assertion NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_head.
- NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_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." NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_provenance.
- NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion evidence source_evidence_literature NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_provenance.
- NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion SIO_000772 20586826 NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_provenance.
- NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion wasDerivedFrom gad-20150221 NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_provenance.
- NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion wasGeneratedBy ECO_0000203 NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_provenance.