Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion evidence source_evidence_literature NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion SIO_000772 17952667 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion wasDerivedFrom befree-20140225 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion wasGeneratedBy ECO_0000203 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.