Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion type Assertion NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_head.
- NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion wasGeneratedBy ECO_0000203 NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_provenance.
- NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion wasDerivedFrom befree-20140225 NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_provenance.
- NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion SIO_000772 9006320 NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_provenance.
- NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion evidence source_evidence_literature NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_provenance.
- NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_assertion description "[The tuberous sclerosis-2 (TSC2) gene is linked to tuberous sclerosis (TSC), a dominantly inherited genetic syndrome in which inactivation of the normal TSC2 allele is associated with the development of mostly benign tumors and focal dysplasias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655695.RANoOqa6EFFnd7SWeK4Hz5qthkcx6x1G4C2cc1dnHyVoA130_provenance.