Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_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." NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_assertion evidence source_evidence_literature NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_assertion SIO_000772 20586826 NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_assertion wasDerivedFrom gad-20150221 NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_assertion wasGeneratedBy ECO_0000203 NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.