Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion> ?p ?o ?g. }
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- NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion type Assertion NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_head.
- NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion description "[Despite the fact that the frequency of TMIE variants in our study subjects was low, we suggested that c.257G>A (p.R86Q) variant is a de novo and may be as a risk factor for the development of hearing loss in Taiwanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_provenance.
- NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion evidence source_evidence_literature NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_provenance.
- NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion SIO_000772 20206386 NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_provenance.
- NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion wasDerivedFrom gad-20150221 NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_provenance.
- NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_assertion wasGeneratedBy ECO_0000203 NP140855.RAOaARRThsbMiXAnggR2_64pYBKZzvG_ES1ukclpNldPg130_provenance.