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- source_evidence_literature type ECO_0000212 NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_assertion description "[The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_assertion evidence source_evidence_literature NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_assertion SIO_000772 25720245 NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_assertion wasDerivedFrom befree-2016 NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_assertion wasGeneratedBy ECO_0000203 NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266490.RAZgKLUZ8kSi8lpUsQf1XjYycg7-Dwlo2sBJ7AQBlS6R0130_provenance.