Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion type Assertion NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_head.
- NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion description "[Deletions of GJB6, which encodes connexin 30, cause SNHL in a digenic manner with a heterozygous GJB2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_provenance.
- NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion evidence source_evidence_literature NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_provenance.
- NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion SIO_000772 19877196 NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_provenance.
- NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion wasDerivedFrom befree-2016 NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_provenance.
- NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_assertion wasGeneratedBy ECO_0000203 NP772770.RApY3a_e6NO91SifUY8Sy-6raorOz_saeRtTBB1aS17-o130_provenance.