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- source_evidence_literature type ECO_0000212 NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_assertion wasGeneratedBy ECO_0000203 NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_assertion wasDerivedFrom befree-20150227 NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_assertion SIO_000772 19027966 NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_assertion evidence source_evidence_literature NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.
- NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_assertion description "[In the years 2005-2007 we have screened 194 probands with early onset hearing loss and 68 family members with an arrayed primer extension (APEX) microarray, which covers 201 mutations in six nuclear genes (GJB2, GJB6, GJB3, GJA1, SLC26A4, SLC26A5) and two mitochondrial genes encoding 12S rRNA and tRNA-Ser (UCN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765435.RAnYbISZ4EtGSr_-kI5YUP6C9Yk8T6MhLGWnKhDUuIurM130_provenance.