Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP927792.RAk2hSMWc7dm9DHNsY0xR_SB3KCRrmtoE_imy8qKmboEs130_provenance.