Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion> ?p ?o ?g. }
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- NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion type Assertion NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_head.
- NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion description "[Participants were 36 subjects, ranging between 30 and 60 years, who were divided into two groups: a control group composed by individuals without auditory complaints and without family history of hearing loss, and a research group composed by heterozygous parents of individuals with autosomal recessive hearing loss or heterozygous for connexin 26 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_provenance.
- NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion evidence source_evidence_literature NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_provenance.
- NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion SIO_000772 21271090 NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_provenance.
- NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion wasDerivedFrom befree-2016 NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_provenance.
- NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_assertion wasGeneratedBy ECO_0000203 NP868123.RAtEivpQidj1O1MYVQfYLCXSq9nMDWiF1Bmakn_95tZBM130_provenance.