Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion type Assertion NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_head.
- NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion description "[Mutations in CRB1 are associated with a range of recessively inherited retinal dystrophies, including LCA, childhood- and juvenile-onset rod-cone and cone-rod dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion evidence source_evidence_literature NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion SIO_000772 20956273 NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion wasDerivedFrom befree-2016 NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_assertion wasGeneratedBy ECO_0000203 NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.