Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_assertion evidence source_evidence_literature NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_assertion SIO_000772 16806828 NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_assertion wasDerivedFrom befree-2016 NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_assertion wasGeneratedBy ECO_0000203 NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.
- befree-2016 importedOn "2016-02-19" NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.