Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_assertion description "[The genotype and/or allele frequencies of 6 tag SNPs in CRP, ecNOS, PC-1 and ACE genes were significantly different between CAD and control groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_assertion evidence source_evidence_literature NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_assertion SIO_000772 21119571 NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_assertion wasDerivedFrom gad-20130706 NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_assertion wasGeneratedBy ECO_0000203 NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87927.RAaQgn9Y4NQqyJ4ENpe3S1QaupFq7wwRrmY_cYNGOC72g130_provenance.