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- source_evidence_literature type ECO_0000212 NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_assertion evidence source_evidence_literature NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_assertion SIO_000772 10802646 NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_assertion wasDerivedFrom befree-20140225 NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_assertion wasGeneratedBy ECO_0000203 NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889833.RAxgiEGw6GaktRUViqf7V5aVot1hz1veB4YiEK4m-E3JY130_provenance.