Matches in Nanopublications for { ?s ?p "[Therefore, the authors' data provide supportive evidence that mutations in the coding region of the NKX2-5 gene and sequence variants within its promoter region may be among the contributors to the CHD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion description "[Therefore, the authors' data provide supportive evidence that mutations in the coding region of the NKX2-5 gene and sequence variants within its promoter region may be among the contributors to the CHD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion description "[Therefore, the authors' data provide supportive evidence that mutations in the coding region of the NKX2-5 gene and sequence variants within its promoter region may be among the contributors to the CHD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_provenance.
- NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_assertion description "[Therefore, the authors' data provide supportive evidence that mutations in the coding region of the NKX2-5 gene and sequence variants within its promoter region may be among the contributors to the CHD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.