Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.