Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_assertion description "[OPA1 gene sequencing in patients with hereditary optic neuropathies indicates that the clinical spectrum of ADOA is larger than previously thought.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_assertion evidence source_evidence_literature NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_assertion SIO_000772 19389487 NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_assertion wasDerivedFrom befree-2016 NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_assertion wasGeneratedBy ECO_0000203 NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.
- befree-2016 importedOn "2016-02-19" NP734324.RAfwklilSsy2ZPhb4mvGV_eEyzmXUOLKQLiLYiuAk32uw130_provenance.