Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_assertion description "[We evaluated patients with hereditary retinal diseases featuring subretinal spots (retinitis punctata albescens and fundus albipunctatus) and patients with typical dominant or recessive retinitis pigmentosa for mutations in RDH5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_assertion evidence source_evidence_literature NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_assertion SIO_000772 10369264 NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_assertion wasDerivedFrom befree-2016 NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_assertion wasGeneratedBy ECO_0000203 NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.
- befree-2016 importedOn "2016-02-19" NP255055.RATxLM3KTdJrAGurKo8M66v9JuLS_7YIhPshrBLjrm9pY130_provenance.