Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion type Assertion NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_head.
- NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion wasGeneratedBy ECO_0000203 NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_provenance.
- NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion wasDerivedFrom befree-2016 NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_provenance.
- NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion SIO_000772 23687350 NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_provenance.
- NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion evidence source_evidence_literature NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_provenance.
- NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_assertion description "[Mutations in TSC1 or TSC2 cause the tuberous sclerosis complex (TSC), a disorder characterised by the development of hamartomas or benign tumours in various organs as well as the variable presence of epilepsy, intellectual disability (ID) and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1078953.RAh61nzUHcDLCaBIOO3YTU3DNW4vkQgxVKm07qe2F-hO4130_provenance.