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- source_evidence_literature type ECO_0000212 NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_assertion description "[Heterozygous mutations in the X-linked MECP2 gene cause Rett syndrome, a severe neurodevelopmental disorder of young females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_assertion evidence source_evidence_literature NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_assertion SIO_000772 10986043 NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_assertion wasDerivedFrom befree-2016 NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_assertion wasGeneratedBy ECO_0000203 NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.
- befree-2016 importedOn "2016-02-19" NP294996.RAeYWLtDo47RvtAvZMmv8Hq-EYWSAgHRLuVJDovoqWdj0130_provenance.