Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion type Assertion NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_head.
- 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.
- NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion evidence source_evidence_literature NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion SIO_000772 22576768 NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion wasDerivedFrom befree-20140225 NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_assertion wasGeneratedBy ECO_0000203 NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.