Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_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." NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_assertion evidence source_evidence_literature NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_assertion SIO_000772 7545545 NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_assertion wasDerivedFrom befree-20150227 NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_assertion wasGeneratedBy ECO_0000203 NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387017.RALOvclWIN89Gwf6UToUQQC46l0jBOBfVs5D_nHC4zZtE130_provenance.