Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_assertion evidence source_evidence_literature NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_assertion SIO_000772 10320095 NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_assertion wasDerivedFrom befree-20140225 NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_assertion wasGeneratedBy ECO_0000203 NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.