Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion> ?p ?o ?g. }
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- NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion type Assertion NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_head.
- NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion description "[a MECP2 mutation associated with Rett syndrome in females could lead to a similar phenotype in males as a result of somatic mosaicism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_provenance.
- NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion evidence source_evidence_literature NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_provenance.
- NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion SIO_000772 11896459 NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_provenance.
- NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion wasDerivedFrom lhgdn-20090331 NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_provenance.
- NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_assertion wasGeneratedBy ECO_0000203 NP193617.RAdfGtYnfDCcqejnUtBkT4OgUBc5WJWg3pjv_nXjzQOUQ130_provenance.