Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- befree-2016 importedOn "2016-02-19" NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_assertion wasGeneratedBy ECO_0000203 NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_assertion wasDerivedFrom befree-2016 NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_assertion SIO_000772 22212387 NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_assertion evidence source_evidence_literature NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.
- NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_assertion description "[Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive disorder characterized by 2,8-dihydroxyadenine (2,8-DHA) crystalluria that can cause nephrolithiasis and chronic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950413.RAbOXpcgsYHlv04evZRrUl2PIKPvSlyOiYbgWeXbl7g18130_provenance.