Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion> ?p ?o ?g. }
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- NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion type Assertion NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_head.
- NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion wasGeneratedBy ECO_0000203 NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion wasDerivedFrom befree-2016 NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion SIO_000772 12798584 NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion evidence source_evidence_literature NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_assertion description "[We sought to examine the importance of mutations in the cardiac transcription factor gene NKX2-5 in patients with an atrial septal defect (ASD), patent foramen ovale (PFO), or hypoplastic left heart syndrome (HLHS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.