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- source_evidence_literature type ECO_0000212 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion evidence source_evidence_literature NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion SIO_000772 10496225 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion wasDerivedFrom befree-2016 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion wasGeneratedBy ECO_0000203 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- befree-2016 importedOn "2016-02-19" NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.