Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_assertion description "[11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_assertion evidence source_evidence_curated NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_assertion SIO_000772 10617778 NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_assertion wasDerivedFrom uniprot-2016 NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_assertion wasGeneratedBy ECO_0000218 NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP568.RA-m7-Nx7D4wJy49jgKmfuVUraPyiKo_5P_aAIC5Lk0fE130_provenance.