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- source_evidence_literature type ECO_0000212 NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_assertion description "[Recently, mutations in the mitochondrial translation optimization factor 1 gene (MTO1) were identified as causative in children with hypertrophic cardiomyopathy, lactic acidosis and respiratory chain defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_assertion evidence source_evidence_literature NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_assertion SIO_000772 25506927 NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_assertion wasDerivedFrom befree-2016 NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_assertion wasGeneratedBy ECO_0000203 NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248168.RADwRBdu-2TYZFyaBSTzqm0cHOKeIcqTeUVJMPdcRvEAU130_provenance.