Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion> ?p ?o ?g. }
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- NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion type Assertion NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_head.
- NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion wasGeneratedBy ECO_0000203 NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_provenance.
- NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion wasDerivedFrom befree-20140225 NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_provenance.
- NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion SIO_000772 19027966 NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_provenance.
- NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion evidence source_evidence_literature NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_provenance.
- NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_assertion description "[The aim of our study was to identify the IVS2-2A>G sequence change in the SLC26A5 (Prestin) gene in Estonian individuals with hearing loss and in their family members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699692.RACq9tJ8axCh1fsMhpV_A8PdwVNyjtt6KSILPvg2ir89o130_provenance.