Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_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." NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_assertion evidence source_evidence_literature NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_assertion SIO_000772 7545545 NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_assertion wasDerivedFrom befree-20140225 NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_assertion wasGeneratedBy ECO_0000203 NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.
- befree-20140225 importedOn "2014-02-25" NP521075.RAvBt-d-w6pfMVszlww0sUQ1dE4VbVe-tCVhdxLAxC7Ag130_provenance.