Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_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." NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion evidence source_evidence_literature NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion SIO_000772 11810270 NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion wasDerivedFrom befree-20150227 NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion wasGeneratedBy ECO_0000203 NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.