Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_assertion description "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_assertion evidence source_evidence_literature NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_assertion SIO_000772 17013611 NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_assertion wasDerivedFrom befree-20140225 NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_assertion wasGeneratedBy ECO_0000203 NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.