Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_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." NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_assertion evidence source_evidence_literature NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_assertion SIO_000772 7545545 NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_assertion wasDerivedFrom befree-20140225 NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_assertion wasGeneratedBy ECO_0000203 NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP475448.RA0hNCrRNHu0Vv5EvO5FjDU6UcoQOwPx3iffa74UcGIRc130_provenance.