Matches in Nanopublications for { ?s ?p "[ NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death. It is the second de novo mutation identified in NKX2.5. (2) NKX2.5 mutations are rare in sporadic CHD patients. (3) This study for the first time identifies association between]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP142991.RAZ7HfhWb-oyaucbLVbFGVwbGwdl104917GXToJyxjDJg130_assertion description "[ NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death. It is the second de novo mutation identified in NKX2.5. (2) NKX2.5 mutations are rare in sporadic CHD patients. (3) This study for the first time identifies association between]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142991.RAZ7HfhWb-oyaucbLVbFGVwbGwdl104917GXToJyxjDJg130_provenance.
- NP142992.RA1IEejZHmRQsnzTY2PjDoF0BKOFNtF_K5ZT5ReL2pZl0130_assertion description "[ NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death. It is the second de novo mutation identified in NKX2.5. (2) NKX2.5 mutations are rare in sporadic CHD patients. (3) This study for the first time identifies association between]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142992.RA1IEejZHmRQsnzTY2PjDoF0BKOFNtF_K5ZT5ReL2pZl0130_provenance.
- NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_assertion description "[ NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death. It is the second de novo mutation identified in NKX2.5. (2) NKX2.5 mutations are rare in sporadic CHD patients. (3) This study for the first time identifies association between]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187087.RA-h8iEYnr1izUJUH9wobai8NhuOFLvS8PI_ZDwvM8vvo130_provenance.
- NP187088.RA64LvHZEJJt4jyvEZQY5FMdhIlKj6xtQWcmmfMmGCCBQ130_assertion description "[ NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death. It is the second de novo mutation identified in NKX2.5. (2) NKX2.5 mutations are rare in sporadic CHD patients. (3) This study for the first time identifies association between]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187088.RA64LvHZEJJt4jyvEZQY5FMdhIlKj6xtQWcmmfMmGCCBQ130_provenance.