Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion> ?p ?o ?g. }
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- NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion type Assertion NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_head.
- NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion description "[The patients analyzed included 52 with autosomal dominant retinitis pigmentosa, 36 with autosomal recessive retinitis pigmentosa, 3 with simplex retinitis pigmentosa, 12 with cone-rod dystrophy, 5 with rod-cone dystrophy, 3 with vitelliform macular dystrophy (Best's disease), 4 with macular dystrophy, 2 with cone dystrophy, 2 with fundus flavimaculatus, 2 with fundus albipunctatus, and 12 with retinitis pigmentosa with macular degeneration as well as 40 unrelated normal persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_provenance.
- NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion evidence source_evidence_literature NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_provenance.
- NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion SIO_000772 9690896 NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_provenance.
- NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion wasDerivedFrom befree-2016 NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_provenance.
- NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_assertion wasGeneratedBy ECO_0000203 NP1401025.RAk0VOCQL0NEXre9r_MmiK6PDR0v9SBxtIfyRAVwPe8WY130_provenance.