Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion> ?p ?o ?g. }
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- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion type Assertion NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_head.
- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion evidence source_evidence_literature NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion SIO_000772 12687499 NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion wasDerivedFrom befree-20140225 NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion wasGeneratedBy ECO_0000203 NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.