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- source_evidence_literature type ECO_0000212 NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_assertion description "[The DFNA2 locus for autosomal dominant nonsyndromic hearing impairment on chromosome 1p34 contains at least 2 genes responsible for hearing loss, GJB3 and KCNQ4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_assertion evidence source_evidence_literature NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_assertion SIO_000772 10925378 NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_assertion wasDerivedFrom befree-2016 NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_assertion wasGeneratedBy ECO_0000203 NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.
- befree-2016 importedOn "2016-02-19" NP290796.RA6LlPGitj7f6vyvuH9_45QftE707V6fnNUsiAb7pftFA130_provenance.