Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_assertion description "[Novel SLC5A2 variants contribute to renal glucosuria in Chinese families: abnormal expression and dysfunction of variant SLC5A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_assertion evidence source_evidence_literature NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_assertion SIO_000772 25339128 NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_assertion wasDerivedFrom befree-2016 NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_assertion wasGeneratedBy ECO_0000203 NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231882.RAepWgOEena7eJ4Qxd2e3p8trvACD4nYCW3Sse9Sn0Vus130_provenance.