Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion> ?p ?o ?g. }
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- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion type Assertion NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_head.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion description "[it is reported for the first time that mutations in CABP4 lead to autosomal recessive congenital stationary night blindness]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion evidence source_evidence_literature NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion SIO_000772 16960802 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion wasDerivedFrom lhgdn-20090331 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion wasGeneratedBy ECO_0000203 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.