Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion> ?p ?o ?g. }
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- NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion type Assertion NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_head.
- NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion description "[Mutations in the retinitis pigmentosa 1 (RP1) gene are a common cause of autosomal dominant retinitis pigmentosa (adRP), and have also been found to cause autosomal recessive RP (arRP) in a few families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_provenance.
- NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion evidence source_evidence_literature NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_provenance.
- NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion SIO_000772 22927954 NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_provenance.
- NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion wasDerivedFrom befree-2016 NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_provenance.
- NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_assertion wasGeneratedBy ECO_0000203 NP1008602.RA7Anx2a6HWLgyfdg6o41C-68NFv8AjfZ385rBta0Xnl8130_provenance.