Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_assertion description "[These findings demonstrate that both retinitis pigmentosa and macular dystrophies are caused by mutations in RDS and that the functional significance of certain amino-acids in peripherin-RDS may be different in cones and rods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_assertion evidence source_evidence_literature NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_assertion SIO_000772 8485576 NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_assertion wasDerivedFrom befree-2016 NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_assertion wasGeneratedBy ECO_0000203 NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1343027.RAU39py62kF3aKb_vM_LpR2y1eoO9NDeKR1Gc6wk2RrwE130_provenance.