Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion type Assertion NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_head.
- NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion description "[Sequencing of the entire GJB2 gene-coding region in Czech patients with pre-lingual bilateral hearing loss revealed that 10.3% of Czech patients carry only one monoallelic pathogenic mutation in the coding region of the GJB2 gene, which is significantly more than the population frequency of 3.4%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_provenance.
- NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion evidence source_evidence_literature NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_provenance.
- NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion SIO_000772 16650079 NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_provenance.
- NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion wasDerivedFrom befree-20140225 NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_provenance.
- NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_assertion wasGeneratedBy ECO_0000203 NP856586.RAHwagHUOldu8Nv4T7qJWCvV5Q1_LIVNVd7_cHVo53Fu8130_provenance.