Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion description "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion evidence source_evidence_literature NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion SIO_000772 16261627 NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion wasDerivedFrom befree-20140225 NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion wasGeneratedBy ECO_0000203 NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.