Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion type Assertion NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_head.
- NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion description "[Twelve distinct mutations in the NKX2.5 coding region were identified in 18 of 608 patients (3%), including 9 of 201 (4%) with tetralogy of Fallot, 3 of 71 (4%) with a secundum ASD, one each with truncus arteriosus, double-outlet right ventricle, L-transposition of the great arteries, interrupted aortic arch, hypoplastic left heart syndrome, and aortic coarctation, but in no patients with D-transposition of the great arteries (n = 86) or valvar aortic stenosis (n = 21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_provenance.
- NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion evidence source_evidence_literature NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_provenance.
- NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion SIO_000772 14607454 NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_provenance.
- NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion wasDerivedFrom befree-2016 NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_provenance.
- NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_assertion wasGeneratedBy ECO_0000203 NP419882.RAIeRHgxv5nFmw0gs4PXhphHQ_kU2DQKyuzsiI080dN0s130_provenance.