Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion type Assertion NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_head.
- NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion description "[The 342-kb deletion [del(GJB6-D13S1830)] of the Cx30 gene is the second most common connexin mutation after the 35delG mutation in some NSHL populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_provenance.
- NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion evidence source_evidence_literature NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_provenance.
- NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion SIO_000772 18554165 NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_provenance.
- NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion wasDerivedFrom befree-20150227 NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_provenance.
- NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_assertion wasGeneratedBy ECO_0000203 NP1012309.RAyOiBIGI2Fu8fjr1HlLZAFQR0ZpB-a1nMgmrTvkRKWwU130_provenance.