Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_assertion evidence source_evidence_literature NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_assertion SIO_000772 10739753 NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_assertion wasDerivedFrom befree-20150227 NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_assertion wasGeneratedBy ECO_0000203 NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.