Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251690.RA7PrUaPUcHq54i5J6zKbAMAuz-x_1z_OZ_75bz8l-0Nk#provenance>. }
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- source_evidence_literature type ECO_0000212 provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." provenance.
- LHGDN importedOn "2009-03-31" provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom LHGDN provenance.
- assertion SIO_000772 12798584 provenance.
- assertion evidence source_evidence_literature provenance.
- assertion description "[NKX2-5 mutations are a relatively infrequent cause of sporadic ASD (atrial septal defect) and HLHS (hypoplastic left heart syndrome)/for NKX2-5 mutations warranted in individuals with ASD family history, irrespective of AV conduction block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.