Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_assertion evidence source_evidence_literature NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_assertion SIO_000772 11389483 NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_assertion wasDerivedFrom befree-2016 NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_assertion wasGeneratedBy ECO_0000203 NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
- befree-2016 importedOn "2016-02-19" NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.