Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion evidence source_evidence_literature NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion SIO_000772 11810270 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion wasDerivedFrom befree-2016 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion wasGeneratedBy ECO_0000203 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.