Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion type Assertion NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_head.
- NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion description "[Mutations in SLC26A4 cause nonsyndromic hearing loss associated with an enlarged vestibular aqueduct (EVA, also known as DFNB4) and Pendred syndrome (PS), the most common type of autosomal-recessive syndromic deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_provenance.
- NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion evidence source_evidence_literature NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_provenance.
- NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion SIO_000772 19426954 NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_provenance.
- NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion wasDerivedFrom befree-20140225 NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_provenance.
- NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_assertion wasGeneratedBy ECO_0000203 NP577874.RA7aQ6Um2EfjwPNoylgaxO9CrfzvyQlIcxRLs4K1Ki3ys130_provenance.