Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_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." NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_assertion evidence source_evidence_literature NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_assertion SIO_000772 17952667 NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_assertion wasDerivedFrom befree-20140225 NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_assertion wasGeneratedBy ECO_0000203 NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807689.RArxUCuk4RQQBHHV7WG-bqoo4GUW9oHyR1LT8lN_oUBq0130_provenance.