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- source_evidence_literature type ECO_0000212 NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- befree-2016 importedOn "2016-02-19" NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_assertion wasGeneratedBy ECO_0000203 NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_assertion wasDerivedFrom befree-2016 NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_assertion SIO_000772 17309881 NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_assertion evidence source_evidence_literature NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.
- NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_assertion description "[Rett syndrome (RTT) is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in the MECP2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.