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- source_evidence_literature type ECO_0000212 NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in a]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_assertion evidence source_evidence_literature NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_assertion SIO_000772 20591486 NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_assertion wasDerivedFrom gad-20150221 NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_assertion wasGeneratedBy ECO_0000203 NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180178.RApiwST3M_3rqMY6nUImYldu4y7ijkMez3LlF0fPXmI9I130_provenance.