Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_assertion description "[As studies are lacking in North-West Indian Punjabi's, a distinct ethnic group with high incidence of CAD, we determined PON1 activity, genotypes and haplotypes in this population and correlated them with the risk of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_assertion evidence source_evidence_curated NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_assertion SIO_000772 21629682 NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_assertion wasDerivedFrom ctd_human-20150221 NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_assertion wasGeneratedBy ECO_0000218 NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP26653.RAqvPRsI6LvPjFEjCWw1trgsWU2aAKBrsn9y2pJv9YCbQ130_provenance.