Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion type Assertion NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_head.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion description "[Mutations in GJB2 encoding the gap junction protein connexin-26 (Cx26) have been established as the basis of autosomal recessive non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion evidence source_evidence_literature NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion SIO_000772 9856479 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion wasDerivedFrom befree-2016 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion wasGeneratedBy ECO_0000203 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.