Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_assertion description "[Here, we identify mutations in Gipc3 underlying progressive sensorineural hearing loss (age-related hearing loss 5, ahl5) and audiogenic seizures (juvenile audiogenic monogenic seizure 1, jams1) in mice and autosomal recessive deafness DFNB15 and DFNB95 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_assertion evidence source_evidence_literature NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_assertion SIO_000772 21326233 NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_assertion wasDerivedFrom befree-20150227 NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_assertion wasGeneratedBy ECO_0000203 NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968562.RAAgEZZBnW5aVauAcMY5EWVqQJRlZwS9M8U5ZqqcBYsJo130_provenance.