Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_assertion description "[Seven missense mutations and one in-frame deletion mutation have been reported in the coagulation factor C homology (COCH) gene, causing the adult-onset, progressive sensorineural hearing loss and vestibular disorder at the DFNA9 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_assertion evidence source_evidence_literature NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_assertion SIO_000772 16481359 NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_assertion wasDerivedFrom befree-20140225 NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_assertion wasGeneratedBy ECO_0000203 NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616848.RAhwN2oB6gjfws96aG8pZ69SI8ydFbANVJPHrla8UwLAY130_provenance.