Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_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." NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- NP153540.RA6NFUTwRTdfGDfr7hy2Qh8nxTWAvRmIPRizOEUyqveaA130_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." NP153540.RA6NFUTwRTdfGDfr7hy2Qh8nxTWAvRmIPRizOEUyqveaA130_provenance.
- NP216647.RA4l67kePO7EkUOtAs8-ZbXdPps2W1HDXX_oqemjOdjAk130_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." NP216647.RA4l67kePO7EkUOtAs8-ZbXdPps2W1HDXX_oqemjOdjAk130_provenance.
- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_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." NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_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.
- 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.
- NP214368.RAncdLpOyvIGHLEMmp0TQxYnK-b5Fad69XarqcViT6H_Y130_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." NP214368.RAncdLpOyvIGHLEMmp0TQxYnK-b5Fad69XarqcViT6H_Y130_provenance.
- NP200060.RAFUGbUn8JKcDFhiv64NeE3ABLTF3JJRMzxy6V8YvH7q4130_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." NP200060.RAFUGbUn8JKcDFhiv64NeE3ABLTF3JJRMzxy6V8YvH7q4130_provenance.