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- source_evidence_literature type ECO_0000212 NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_assertion description "[The purpose of this study was to determine the prevalence of mutations in the peripherin/RDS gene in Spanish patients with different types of autosomal dominant macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_assertion evidence source_evidence_literature NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_assertion SIO_000772 17653047 NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_assertion wasDerivedFrom befree-20150227 NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_assertion wasGeneratedBy ECO_0000203 NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760993.RAAuWSw7qgpSPFawleL-2vwzLTtYr9SXV2s2oCVvTYL7Q130_provenance.