Matches in Nanopublications for { ?s ?p "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_provenance.
- NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_provenance.
- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_provenance.