Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_assertion> ?p ?o ?g. }
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- NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_assertion type Assertion NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_head.
- NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_assertion wasGeneratedBy ECO_0000203 NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_provenance.
- NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_assertion wasDerivedFrom befree-2016 NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_provenance.
- NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_assertion SIO_000772 23687350 NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_provenance.
- NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_assertion evidence source_evidence_literature NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_provenance.
- NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_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." NP1078946.RAYv5GKxQc6fDDs5jjyJTeBEmm8k97A1zcbJYbosDinZE130_provenance.