Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_assertion description "[A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_assertion evidence source_evidence_literature NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_assertion SIO_000772 22058112 NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_assertion wasDerivedFrom befree-20150227 NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_assertion wasGeneratedBy ECO_0000203 NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP854783.RAdqYoQ7Cj7xWF7r6zh_aMDyV5CS3XOwDHJYYE4zf0Tlc130_provenance.