Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion> ?p ?o ?g. }
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- NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion type Assertion NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_head.
- NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_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." NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_provenance.
- NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion evidence source_evidence_literature NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_provenance.
- NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion SIO_000772 10320095 NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_provenance.
- NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion wasDerivedFrom befree-20140225 NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_provenance.
- NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion wasGeneratedBy ECO_0000203 NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_provenance.