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- source_evidence_literature type ECO_0000212 NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_assertion description "[Accordingly, enhanced activity of ADAM17�in cartilage, caused by the expression of the rare double sFRP3 variant, provides an explanation for the genetic effect of sFRP3 variants in joint disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_assertion evidence source_evidence_literature NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_assertion SIO_000772 25846075 NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_assertion wasDerivedFrom befree-2016 NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_assertion wasGeneratedBy ECO_0000203 NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1276107.RA0Ti41slNEqog_NN572F6BBus6Aep-BjRfP0tLCKlHaI130_provenance.