Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP824596.RAw4MjQe6Z16Gb6JUox7D77cryvpXTIXmp-7wYqFE5UE8130_provenance.