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- source_evidence_literature type ECO_0000212 NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_assertion description "[General mitochondrial trifunctional protein (TFP) deficiency leads to a wide clinical spectrum of disease ranging from severe neonatal/infantile cardiomyopathy and early death to mild chronic progressive sensorimotor poly-neuropathy with episodic rhabdomyolysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_assertion evidence source_evidence_literature NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_assertion SIO_000772 15902556 NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_assertion wasDerivedFrom befree-20140225 NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_assertion wasGeneratedBy ECO_0000203 NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP769289.RAwK9PKnpCEH3o4zdACud2BiEl4wci_3YmHtC-1lkWJW8130_provenance.