Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- befree-2016 importedOn "2016-02-19" NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_assertion wasGeneratedBy ECO_0000203 NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_assertion wasDerivedFrom befree-2016 NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_assertion SIO_000772 10792313 NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_assertion evidence source_evidence_literature NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.
- NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_assertion description "[In the absence of mutation, EDN3 is downregulated in short-segment Hirschsprung disease, suggesting that this may be a common step leading to aganglionosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282768.RA2waXYejxJABgkD_IXLpksDMVV0Htji1e-t532ITFlgA130_provenance.