Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion> ?p ?o ?g. }
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- NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion type Assertion NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_head.
- NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion wasGeneratedBy ECO_0000203 NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_provenance.
- NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion wasDerivedFrom befree-20140225 NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_provenance.
- NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion SIO_000772 21872273 NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_provenance.
- NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion evidence source_evidence_literature NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_provenance.
- NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_assertion description "[Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive disorder characterized by ichthyosis, spastic di- or tetraplegia and mental retardation due a defect of the fatty aldehyde dehydrogenase (FALDH), related to mutations in the ALDH3A2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455302.RABmYeCjyL5oK9eXy3Ojo_wwML1VrVVhEd3e8UjiIfgto130_provenance.