Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion> ?p ?o ?g. }
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- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_assertion type Assertion NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_head.
- 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.