Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_assertion type Assertion NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_head.
- NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_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." NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_provenance.
- NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_assertion evidence source_evidence_literature NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_provenance.
- NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_assertion SIO_000772 20206386 NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_provenance.
- NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_assertion wasDerivedFrom befree-20140225 NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_provenance.
- NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_assertion wasGeneratedBy ECO_0000203 NP422278.RAmykiGTUo0dXSTweUXDggv1LL5mCsLpyt0J2CZ7c3Sck130_provenance.