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- source_evidence_literature type ECO_0000212 NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_assertion description "[In human patients, cortical dysplasia produced by Doublecortin (DCX) mutations lead to mental retardation and intractable infantile epilepsies, but the underlying mechanisms are not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_assertion evidence source_evidence_literature NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_assertion SIO_000772 19144832 NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_assertion wasDerivedFrom befree-2016 NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_assertion wasGeneratedBy ECO_0000203 NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.
- befree-2016 importedOn "2016-02-19" NP714229.RA-e8G-IMWy-GmfU_Uj-U0awN0tRBaZFoY20UNT_UT9Iw130_provenance.