Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion> ?p ?o ?g. }
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- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion type Assertion NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_head.
- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion wasGeneratedBy ECO_0000203 NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_provenance.
- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion wasDerivedFrom gad-20150221 NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_provenance.
- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion SIO_000772 20513142 NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_provenance.
- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion evidence source_evidence_literature NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_provenance.
- NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_assertion description "[the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131185.RA3HCJTSWogDP9AaUTHkv-gKyjhQl6iAyXUCC9ciesVbU130_provenance.