Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion> ?p ?o ?g. }
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- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion type Assertion NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_head.
- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_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." NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_provenance.
- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion evidence source_evidence_literature NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_provenance.
- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion SIO_000772 19806373 NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_provenance.
- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion wasDerivedFrom befree-20150227 NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_provenance.
- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion wasGeneratedBy ECO_0000203 NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_provenance.