Matches in Nanopublications for { ?s ?p "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1553.RAdEVUhcFlAg7_3CSKYJSSI10wlvhWSczq5bXlq79jzxw130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1553.RAdEVUhcFlAg7_3CSKYJSSI10wlvhWSczq5bXlq79jzxw130_provenance.
- NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_provenance.
- NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- NP4384.RApGjjkzxgR6MOrtHHg8RlDXsDIoNx20g3ELgncdHV-Ss130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4384.RApGjjkzxgR6MOrtHHg8RlDXsDIoNx20g3ELgncdHV-Ss130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.