Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_assertion description "[Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_assertion evidence source_evidence_literature NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_assertion SIO_000772 24014202 NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_assertion wasDerivedFrom befree-2016 NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_assertion wasGeneratedBy ECO_0000203 NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108536.RAvQ5MYUWqxSAr8R5LexFn0MImW3n6nJGcjPDzq8Uz7U4130_provenance.