Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion> ?p ?o ?g. }
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- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion type Assertion NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_head.
- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion wasGeneratedBy ECO_0000218 NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_provenance.
- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion wasDerivedFrom uniprot-20130724 NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_provenance.
- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion SIO_000772 19878917 NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_provenance.
- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion evidence source_evidence_curated NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_provenance.
- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_provenance.