Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_assertion description "[Loss-of-function mutations of the MECP2 gene at Xq28 are associated with Rett syndrome in females and with syndromic and nonsyndromic forms of mental retardation (MR) in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_assertion evidence source_evidence_literature NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_assertion SIO_000772 16080119 NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_assertion wasDerivedFrom befree-2016 NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_assertion wasGeneratedBy ECO_0000203 NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.
- befree-2016 importedOn "2016-02-19" NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_provenance.