Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_assertion description "[The CDKL5 gene has been implicated in the molecular etiology of early-onset intractable seizures with infantile spasms (IS), severe hypotonia and atypical Rett syndrome (RTT) features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_assertion evidence source_evidence_literature NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_assertion SIO_000772 19793311 NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_assertion wasDerivedFrom befree-2016 NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_assertion wasGeneratedBy ECO_0000203 NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.
- befree-2016 importedOn "2016-02-19" NP766435.RA3gG-UNt_CHal4ggs02JC-84K2_IXmZ-4e2-OK4w65RE130_provenance.