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- source_evidence_literature type ECO_0000212 NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_assertion description "[Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_assertion evidence source_evidence_literature NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_assertion SIO_000772 21221624 NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_assertion wasDerivedFrom befree-2016 NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_assertion wasGeneratedBy ECO_0000203 NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP864419.RAj12Yiq04FkaaRF9dt1w5B1kVQigmt-xWV81C2I_qjfA130_provenance.