Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP833517.RACYCYj5ya9HWzwJyWyRnxxcIXz7m5svq8VGaQI1t2OWI130_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." NP833517.RACYCYj5ya9HWzwJyWyRnxxcIXz7m5svq8VGaQI1t2OWI130_provenance.
• NP207635.RA6GEWFkCr6z6qLOjThgH9_LWfuIJQwD-6tTuZe2EBejA130_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." NP207635.RA6GEWFkCr6z6qLOjThgH9_LWfuIJQwD-6tTuZe2EBejA130_provenance.
• NP384762.RAC_KACGD10_ln_-pPP_RjdWL9lrZ7hPPq5dQYgJjhcR0130_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." NP384762.RAC_KACGD10_ln_-pPP_RjdWL9lrZ7hPPq5dQYgJjhcR0130_provenance.
• NP184158.RAhSz3SBHc-hu8xZSZPRRZP20ukKwUyzZvB-wL61U7Ynw130_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." NP184158.RAhSz3SBHc-hu8xZSZPRRZP20ukKwUyzZvB-wL61U7Ynw130_provenance.
• NP191014.RAs1zOdIUtSvESUBlJsGGaUOuTaK4lSc4D07jsVMQ31nw130_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." NP191014.RAs1zOdIUtSvESUBlJsGGaUOuTaK4lSc4D07jsVMQ31nw130_provenance.
• NP195202.RAtdpibwGD1XwmiSTLqkHZrokGNee59O8Z-lJ9M5yxnmE130_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." NP195202.RAtdpibwGD1XwmiSTLqkHZrokGNee59O8Z-lJ9M5yxnmE130_provenance.
• NP655486.RApt9bTSDPqRYfHYR616UjklGr2GcayEOVjRDyWivXerg130_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." NP655486.RApt9bTSDPqRYfHYR616UjklGr2GcayEOVjRDyWivXerg130_provenance.
• NP788345.RAgZFav2rJAjibQmlAlnmEskAWYwqaK6n-gl1ttaVUoTs130_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." NP788345.RAgZFav2rJAjibQmlAlnmEskAWYwqaK6n-gl1ttaVUoTs130_provenance.
• NP332935.RA56InbCvUatbs2-5bSNgNEwY2ErN8NwV5sZfZ69kvdmw130_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." NP332935.RA56InbCvUatbs2-5bSNgNEwY2ErN8NwV5sZfZ69kvdmw130_provenance.
• 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.
• NP334033.RAcD1DFXrpzLNZakd6LqDAGTbuUqgol8AFUfl3yA5AK8E130_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." NP334033.RAcD1DFXrpzLNZakd6LqDAGTbuUqgol8AFUfl3yA5AK8E130_provenance.
• NP724379.RA_5LOeNHXhgRQxgk1Qx1gGz-assvtslj5VpiP0T5IgKU130_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." NP724379.RA_5LOeNHXhgRQxgk1Qx1gGz-assvtslj5VpiP0T5IgKU130_provenance.
• NP113071.RAinCH9M32fx4iFmBjH_iNXkGB5eq_sXSeYjUhROH2eb8130_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." NP113071.RAinCH9M32fx4iFmBjH_iNXkGB5eq_sXSeYjUhROH2eb8130_provenance.
• NP811124.RAa5etazWzkjqvJD0GP-FQhNjKJLhnHKzx0sgoikMUEFI130_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." NP811124.RAa5etazWzkjqvJD0GP-FQhNjKJLhnHKzx0sgoikMUEFI130_provenance.
• 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.
• NP811127.RAAEyHade0MqB-Bcn3SdDxpzqY1X37Foh9EzmyvjC05OA130_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." NP811127.RAAEyHade0MqB-Bcn3SdDxpzqY1X37Foh9EzmyvjC05OA130_provenance.
• NP934738.RAO15cHiYz8-_YxMCiDYRUJeejca96qrSfq4gPpL-XXZM130_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." NP934738.RAO15cHiYz8-_YxMCiDYRUJeejca96qrSfq4gPpL-XXZM130_provenance.
• NP334052.RALq9a3ivLRXA9e80oEFFgwftugRuUCuphTTessPt4G3w130_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." NP334052.RALq9a3ivLRXA9e80oEFFgwftugRuUCuphTTessPt4G3w130_provenance.
• NP175808.RA8P6RG2MZxToTuUWJLHQICCLdPNlrumCzDa6m8tR5OQM130_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." NP175808.RA8P6RG2MZxToTuUWJLHQICCLdPNlrumCzDa6m8tR5OQM130_provenance.