Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion> ?p ?o ?g. }
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- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion type Assertion NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_head.
- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_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." NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_provenance.
- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion evidence source_evidence_literature NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_provenance.
- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion SIO_000772 11810270 NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_provenance.
- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion wasDerivedFrom befree-20150227 NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_provenance.
- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion wasGeneratedBy ECO_0000203 NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_provenance.