Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion wasGeneratedBy ECO_0000203 NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion wasDerivedFrom gad-20150221 NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion SIO_000772 15654614 NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion evidence source_evidence_literature NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.
- NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion description "[Interaction analysis of the PROGINS variant with our previously reported associated ESR1 594A variant showed that individuals who possessed at least one copy of both risk alleles were 3.2 times more likely to suffer migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance.