Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_assertion> ?p ?o ?g. }
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- NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_assertion type Assertion NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_head.
- NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_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." NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_provenance.
- NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_assertion evidence source_evidence_literature NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_provenance.
- NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_assertion SIO_000772 19877196 NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_provenance.
- NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_assertion wasDerivedFrom befree-20140225 NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_provenance.
- NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_assertion wasGeneratedBy ECO_0000203 NP438849.RAPjILbzyimsbdRSAvEZZa8tPuwnCtNP5h0kwxy2-4cXI130_provenance.