Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion> ?p ?o ?g. }
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- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion type Assertion NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_head.
- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_provenance.
- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion evidence source_evidence_literature NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_provenance.
- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion SIO_000772 22968132 NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_provenance.
- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion wasDerivedFrom befree-2016 NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_provenance.
- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion wasGeneratedBy ECO_0000203 NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_provenance.