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- source_evidence_literature type ECO_0000212 NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_assertion description "[These results indicate that the KCNJ13 R162W mutation can cause SVD and further show that vitreoretinal degeneration can arise through mutations in genes whose products are not structural components of the vitreous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_assertion evidence source_evidence_literature NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_assertion SIO_000772 18179896 NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_assertion wasDerivedFrom befree-2016 NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_assertion wasGeneratedBy ECO_0000203 NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.
- befree-2016 importedOn "2016-02-19" NP648735.RAU26uBkvap852LlPlB_hMr0xaEYqjtVdNP1ZF-7H94LY130_provenance.