Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion> ?p ?o ?g. }
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- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion type Assertion NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_head.
- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion description "[Recently, the FOXG1 gene was implicated in the molecular aetiology of the congenital variant of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_provenance.
- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion evidence source_evidence_literature NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_provenance.
- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion SIO_000772 19806373 NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_provenance.
- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion wasDerivedFrom befree-20140225 NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_provenance.
- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion wasGeneratedBy ECO_0000203 NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_provenance.