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- source_evidence_literature type ECO_0000212 NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_assertion evidence source_evidence_literature NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_assertion SIO_000772 15466077 NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_assertion wasDerivedFrom befree-20150227 NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_assertion wasGeneratedBy ECO_0000203 NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP220351.RAM9DXYUdc_-s4ojnTBMKD_lIA4XXh-x0eq3RUyxYzWdg130_provenance.