Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_assertion description "[Studies of how TSC1 and TSC2 function in normal and dysplastic cerebral neocortex may provide a paradigm for understanding the neurobiology of other genes that determine epilepsy-associated cerebral malformations (e.g.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_assertion evidence source_evidence_literature NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_assertion SIO_000772 9761305 NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_assertion wasDerivedFrom befree-20140225 NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_assertion wasGeneratedBy ECO_0000203 NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490393.RAl3NzR-b-5v34-hUD-B6GYx4JHDp9L1teptvdgzLEfxo130_provenance.