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- source_evidence_literature type ECO_0000212 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion description "[Mutations in the Connexin 26 (Cx26) gene have been found to account for approximately 20% of all childhood deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion evidence source_evidence_literature NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion SIO_000772 12121355 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion wasDerivedFrom befree-20150227 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion wasGeneratedBy ECO_0000203 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.