Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_assertion description "[6), and mutations in RDS (the human homologue of Prph2) cause retinal degeneration, the relationship of Rom-1 to these processes is uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_assertion evidence source_evidence_literature NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_assertion SIO_000772 10802659 NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_assertion wasDerivedFrom befree-20140225 NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_assertion wasGeneratedBy ECO_0000203 NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615495.RA_G-1cDa6SByzIYe_-dDpWDpKwAUwjuJee8XUSvNHORI130_provenance.