Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion> ?p ?o ?g. }
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- NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion type Assertion NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_head.
- NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion wasGeneratedBy ECO_0000203 NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_provenance.
- NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion wasDerivedFrom befree-2016 NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_provenance.
- NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion SIO_000772 10587520 NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_provenance.
- NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion evidence source_evidence_literature NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_provenance.
- NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_assertion description "[Mutations in human NKX2.5 cause a variety of cardiac anomalies and may account for a clinically significant portion of tetralogy of Fallot and idiopathic AV block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269270.RAueHw0IeTmO1jaGo2qpmZbiuC93beV9A82jxiRYM8cQY130_provenance.