Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_assertion wasGeneratedBy ECO_0000218 NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_assertion wasDerivedFrom ctd_human-2016 NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_assertion SIO_000772 18162506 NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_assertion evidence source_evidence_curated NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.
- NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_assertion description "[Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20972.RACysYeBFRbS7-3srKktx_U2oSsLrn1tyzLQyg_i01nyk130_provenance.