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- NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_assertion type Assertion NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_head.
- NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_assertion description "[Heterozygous mutations in the human transcription factor gene NKX2.5 are associated with either isolated or combined congenital heart disease (CHD), primarily secundum atrial septal defect-II (ASD-II), ventricular septal defect (VSD) or tetralogy of Fallot (TOF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_provenance.
- NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_assertion evidence source_evidence_literature NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_provenance.
- NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_assertion SIO_000772 20456451 NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_provenance.
- NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_assertion wasDerivedFrom befree-2016 NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_provenance.
- NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_assertion wasGeneratedBy ECO_0000203 NP811126.RAbob0B-9igLjDFw06UM7RKQEyrOxvu2477omn8C1WZNE130_provenance.