Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion type Assertion NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_head.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion wasGeneratedBy ECO_0000218 NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_provenance.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion wasDerivedFrom uniprot-20150221 NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_provenance.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion SIO_000772 19878917 NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_provenance.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion evidence source_evidence_curated NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_provenance.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_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." NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_provenance.