Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion> ?p ?o ?g. }
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- NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion type Assertion NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_head.
- NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion evidence source_evidence_literature NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion SIO_000772 10802646 NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion wasDerivedFrom befree-20140225 NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_assertion wasGeneratedBy ECO_0000203 NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.