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- source_evidence_literature type ECO_0000212 NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_assertion description "[Recently, mutations in RPGRIP were found to lead to the retinal dystrophy, Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_assertion evidence source_evidence_literature NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_assertion SIO_000772 12140192 NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_assertion wasDerivedFrom befree-2016 NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_assertion wasGeneratedBy ECO_0000203 NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.
- befree-2016 importedOn "2016-02-19" NP362502.RAsAgK3WEk0Fj4h7_f-B5qebhKq7UzoxnQpPSQGllJSrU130_provenance.