Matches in Nanopublications for { ?s ?p "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1530.RAewDckAg4YOUVhYfIEiK8fQ7iA3Q6xe9YzNZ75Anojdc130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1530.RAewDckAg4YOUVhYfIEiK8fQ7iA3Q6xe9YzNZ75Anojdc130_provenance.
- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_provenance.
- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_provenance.
- assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_provenance.
- NP846506.RA_pKvA6b9WGSqrwOd28SsfEXtnCmflCRydD58PBN_Za8130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846506.RA_pKvA6b9WGSqrwOd28SsfEXtnCmflCRydD58PBN_Za8130_provenance.