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- source_evidence_literature type ECO_0000212 NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.
- NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_assertion description "[In this study, we investigate the prevalence and phenotype/genotype correlation of connexin (CX) gene family variants in a cohort of children with nonsyndromic hearing loss (HL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.
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- NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_assertion wasDerivedFrom befree-2016 NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.
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- befree-2016 importedOn "2016-02-19" NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.