Matches in Nanopublications for { ?s ?p "[Mutations in the crumbs homologue 1 (CRB1) gene cause a specific form of retinitis pigmentosa (RP) that is designated RP12 and is characterized by a preserved para-arteriolar retinal pigment epithelium (PPRPE) and by severe loss of vision at age <20 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_assertion description "[Mutations in the crumbs homologue 1 (CRB1) gene cause a specific form of retinitis pigmentosa (RP) that is designated RP12 and is characterized by a preserved para-arteriolar retinal pigment epithelium (PPRPE) and by severe loss of vision at age <20 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.