Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_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." NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_provenance.
- NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_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." NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_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.
- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_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." NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_provenance.