Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion> ?p ?o ?g. }
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- NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion type Assertion NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_head.
- NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion description "[Since RS is mostly caused by mutations in the MECP2 gene, transgenic animal models such as the Mecp2-deleted (`Mecp2-null`) mouse have been employed to study neurological symptoms and brain function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion evidence source_evidence_literature NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion SIO_000772 17237885 NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion wasDerivedFrom befree-20140225 NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_assertion wasGeneratedBy ECO_0000203 NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.