Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_assertion description "[Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in either of two genes, TSC1 and TSC2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_assertion evidence source_evidence_literature NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_assertion SIO_000772 22169896 NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_assertion wasDerivedFrom befree-2016 NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_assertion wasGeneratedBy ECO_0000203 NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.
- befree-2016 importedOn "2016-02-19" NP946629.RA4vqjEpfKsnRcxMkChDcT-NLJ7TVA-R2w6_rhtY7IMH8130_provenance.