Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_assertion description "[Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_assertion evidence source_evidence_curated NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_assertion SIO_000772 12022040 NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_assertion wasDerivedFrom ctd_human-20150221 NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_assertion wasGeneratedBy ECO_0000218 NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP19917.RATsl9NzL7VXH3UfdnXQasX8HiQyFpHcEAs6aPSv1lRWs130_provenance.