Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_assertion description "[Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_assertion evidence source_evidence_curated NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_assertion SIO_000772 8673138 NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_assertion wasDerivedFrom uniprot-20150221 NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_assertion wasGeneratedBy ECO_0000218 NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1527.RAV1lfbEv2uqYOSoeSSSm85tg_fZlF6m2OdqG2sobw_ok130_provenance.