Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP349889.RA-XFIgAnP7sYidG3MgxYcWmIz03JKdQ3WGkKecZ0Iub4130_provenance.