Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP846508.RAL4mHa3hjAo1qxYwHnpp6ZgGlmesp4l48Gq5KQ15VQpI130_provenance.