Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_assertion description "[Subsequent studies have shown that mutations in ABCA4 can also cause a variety of other retinal dystrophies including cone rod dystrophy and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_assertion evidence source_evidence_literature NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_assertion SIO_000772 18285826 NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_assertion wasDerivedFrom befree-2016 NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_assertion wasGeneratedBy ECO_0000203 NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.
- befree-2016 importedOn "2016-02-19" NP656322.RAYepw1a4f6bbwJVZ2UJ3b_6BSSwd4WIwhQ7y6lMpOvzo130_provenance.