Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_assertion description "[In addition, CRB1 mutations were detected in five of nine patients who had RP with Coats-like exudative vasculopathy, a relatively rare complication of RP that may progress to partial or total retinal detachment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_assertion evidence source_evidence_literature NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_assertion SIO_000772 11389483 NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_assertion wasDerivedFrom befree-20140225 NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_assertion wasGeneratedBy ECO_0000203 NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP279251.RAsHejoXCe0EkhtWBuv1-M3aMazxbguUpOmxWD5nO659s130_provenance.