Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion> ?p ?o ?g. }
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- NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion type Assertion NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_head.
- NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion description "[Loss-of-function mutations in the gene encoding FAM161A were recently discovered as the cause for RP28, an autosomal recessive form of retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_provenance.
- NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion evidence source_evidence_literature NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_provenance.
- NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion SIO_000772 22791751 NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_provenance.
- NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion wasDerivedFrom befree-20140225 NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_provenance.
- NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_assertion wasGeneratedBy ECO_0000203 NP697035.RA8RuHCnih-nbrgbrQDbAgYZ8RyURV4Q9e-QUu1e8yUIA130_provenance.