Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- befree-2016 importedOn "2016-02-19" NP397683.RARtHLIAaUEuSp6PeZ-o3jCgl7xRNcjykuTp-1szMAlPc130_provenance.
- 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.