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- source_evidence_literature type ECO_0000212 NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_assertion description "[Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_assertion evidence source_evidence_literature NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_assertion SIO_000772 18779497 NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_assertion wasDerivedFrom befree-2016 NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_assertion wasGeneratedBy ECO_0000203 NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.
- befree-2016 importedOn "2016-02-19" NP692041.RADFqpuIyoNgI79Zz5hbQ2bc9kpYDTlZ4n72IRKym2488130_provenance.