Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion> ?p ?o ?g. }
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- NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion type Assertion NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_head.
- NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion description "[findings suggest that COCH mutations are unlikely to cause abnormalities in secretion and suggest that extracellular events might cause autosomal dominant sensorineural deafness (DFNA9) pathology ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_provenance.
- NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion evidence source_evidence_literature NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_provenance.
- NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion SIO_000772 12928864 NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_provenance.
- NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion wasDerivedFrom lhgdn-20090331 NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_provenance.
- NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_assertion wasGeneratedBy ECO_0000203 NP209015.RAg6mLHe7g6F926hkZJEl2PM77h7EzugD-N3ka4Hr78QA130_provenance.