Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_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." NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_assertion evidence source_evidence_literature NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_assertion SIO_000772 10320095 NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_assertion wasDerivedFrom befree-2016 NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_assertion wasGeneratedBy ECO_0000203 NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
- befree-2016 importedOn "2016-02-19" NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.