Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_assertion description "[AMD is a complex disorder caused by genetic and environmental factors in which single nucleotide polymorphisms (SNPs) in the genes CFH and LOC387715/HTRA1/ARMS2 have prognostic importance for progression to advanced AMD (with visual loss).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_assertion evidence source_evidence_literature NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_assertion SIO_000772 19015224 NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_assertion wasDerivedFrom befree-2016 NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_assertion wasGeneratedBy ECO_0000203 NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.
- befree-2016 importedOn "2016-02-19" NP704034.RACYdNEjgLwernogS09RZOXPIclGUhc5F8Bmac03mKuBY130_provenance.