Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP251700.RAorfelktFCmFpKjqMt9jo_Po_mf6LIFV9uY3CekfbqjQ#assertion> ?p ?o ?g. }
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- 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." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 20456451 provenance.
- assertion wasDerivedFrom GAD provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.