Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion> ?p ?o ?g. }
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- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion type Assertion NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_head.
- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion wasGeneratedBy ECO_0000218 NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_provenance.
- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion wasDerivedFrom uniprot-2016 NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_provenance.
- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion SIO_000772 19878917 NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_provenance.
- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion evidence source_evidence_curated NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_provenance.
- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_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." NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_provenance.