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- source_evidence_literature type ECO_0000212 NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_assertion description "[An analysis was performed of the regression of the individual hearing threshold on age in the affected persons in a six-generation Dutch family with nonsyndromic autosomal dominant sensorineural hearing loss, which showed linkage to the DFNA2(1p34) region, similar to at least four previously reported nonrelated families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_assertion evidence source_evidence_literature NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_assertion SIO_000772 9432071 NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_assertion wasDerivedFrom befree-20140225 NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_assertion wasGeneratedBy ECO_0000203 NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP703984.RA9I1-zqphRD1EFNvGhEtCjoeI_HkoQXRiRZw_xe85LJA130_provenance.