Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_assertion wasGeneratedBy ECO_0000203 NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_assertion wasDerivedFrom befree-20150227 NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_assertion SIO_000772 18292760 NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_assertion evidence source_evidence_literature NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.
- NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_assertion description "[In further analyses of incident CHD, genotypes carrying the 402H allele were a significant predictor of incident CHD in whites who had hypertension (402YH: HRR 1.19, 95% CI 1.01-1.40; 402HH: HRR 1.28, 95% CI 1.04-1.57).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833800.RAAzJGVPq_HT2BWQA_9OIj-QjmiSWnoKQmStPgomaIw3c130_provenance.