Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_assertion evidence source_evidence_literature NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_assertion SIO_000772 22968132 NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_assertion wasDerivedFrom befree-20150227 NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_assertion wasGeneratedBy ECO_0000203 NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.