Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion> ?p ?o ?g. }
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- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion type Assertion NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_head.
- 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.