Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion type Assertion NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_head.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_provenance.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion evidence source_evidence_literature NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_provenance.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion SIO_000772 19279310 NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_provenance.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion wasDerivedFrom befree-2016 NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_provenance.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion wasGeneratedBy ECO_0000203 NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_provenance.