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- source_evidence_literature type ECO_0000212 NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_assertion wasGeneratedBy ECO_0000203 NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_assertion wasDerivedFrom befree-20150227 NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_assertion SIO_000772 23687350 NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_assertion evidence source_evidence_literature NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.
- NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_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." NP760098.RA36-Lu9wFG29qbZp6fWufM_HsXEXuc9fAC8XhGnwXaQM130_provenance.