Matches in Nanopublications for { ?s ?p "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP251825.RAbxEvm85JjnKmyL0uJEnfiYI9-CpzFE4ejnlAAHuP2UE130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251825.RAbxEvm85JjnKmyL0uJEnfiYI9-CpzFE4ejnlAAHuP2UE130_provenance.
- NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP334034.RAmoywYwzobT18r3tisrn5V_g0DvUk55aq9d7LyMgfl-I130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334034.RAmoywYwzobT18r3tisrn5V_g0DvUk55aq9d7LyMgfl-I130_provenance.
- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_provenance.
- NP828248.RA73-0_ofd3OChX4Mr2KgX6ZvIWfV76FXca0KKwBb8oK4130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828248.RA73-0_ofd3OChX4Mr2KgX6ZvIWfV76FXca0KKwBb8oK4130_provenance.