Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_assertion description "[Patients with the genetic disorder ataxia telangiectasia (AT) have mutations in the AT mutated (ATM) gene, which is homologous to TEL1 and the checkpoint gene MEC1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_assertion evidence source_evidence_literature NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_assertion SIO_000772 7545545 NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_assertion wasDerivedFrom befree-20150227 NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_assertion wasGeneratedBy ECO_0000203 NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257314.RAGAyyAYYIJk87HW2su8OZIe3nJxETbGABrd6g3RXDb4E130_provenance.