Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_assertion description "[The commonest genetic form of juvenile or early adult onset macular degeneration is Stargardt Disease (STGD) caused by recessive mutations in the gene ABCA4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_assertion evidence source_evidence_literature NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_assertion SIO_000772 22863181 NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_assertion wasDerivedFrom befree-20150227 NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_assertion wasGeneratedBy ECO_0000203 NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP218921.RAavcTkPOCgY2ItNpR_ZApYrH2DJFzRiS5XWxIcz5MNcA130_provenance.