Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_assertion wasGeneratedBy ECO_0000203 NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_assertion wasDerivedFrom befree-20140225 NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_assertion SIO_000772 22998673 NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_assertion evidence source_evidence_literature NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_assertion description "[It is now clearly emerging that epilepsy has distinctive characteristics in typical Rett syndrome and in the different syndromes caused by CDKL5 and FOXG1 gene alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625641.RAiMIXzI0LTMaZxsx_uLasg6K8xJxKhTXvlM-2zMplchk130_provenance.