Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_assertion description "[In the present study, we analyzed the association between AMD and the -576G>A polymorphism of the transferrin gene or the 1892C>T polymorphism of the transferrin receptor 2 (TFR2) gene in 278 patients with AMD and 105 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_assertion evidence source_evidence_literature NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_assertion SIO_000772 21422745 NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_assertion wasDerivedFrom befree-2016 NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_assertion wasGeneratedBy ECO_0000203 NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP881050.RAGoDztOmIF0s8b2_qNVHOCAFEZV9ZLIlmSnan8rrQEIM130_provenance.