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- source_evidence_literature type ECO_0000212 NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_assertion description "[Haploinsufficient GATA4 may show variable expressivity with a wide spectrum of clinical findings, including CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_assertion evidence source_evidence_literature NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_assertion SIO_000772 21933911 NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_assertion wasDerivedFrom befree-20140225 NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_assertion wasGeneratedBy ECO_0000203 NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.
- befree-20140225 importedOn "2014-02-25" NP373733.RA2FEKcr7WrhhcG_-pfgfkEsJK1CCBZzaXFf72D2gJG24130_provenance.