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- NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_assertion type Assertion NP507359.RAIqTbpps4jmJshrX3n2lWQiwLqmd8LX52KWhyEcThlTM130_head.
- 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.