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- source_evidence_literature type ECO_0000212 NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_assertion evidence source_evidence_literature NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_assertion SIO_000772 11309367 NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_assertion wasDerivedFrom befree-2016 NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_assertion wasGeneratedBy ECO_0000203 NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- befree-2016 importedOn "2016-02-19" NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.