Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
• NP11146.RA2bwDsryKsPX-unUmXtQ77rwvzAv4QT9usvOyVt3Rbto130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11146.RA2bwDsryKsPX-unUmXtQ77rwvzAv4QT9usvOyVt3Rbto130_provenance.
• NP11151.RA5zKzYVGA96wz2bAzJnmEkUN9I-yob5macQdRYOyheio130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11151.RA5zKzYVGA96wz2bAzJnmEkUN9I-yob5macQdRYOyheio130_provenance.
• NP11148.RAvj5MTAPg-4sH30TtK9CFD0AEriID2iGjbdGhcfa0aLQ130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11148.RAvj5MTAPg-4sH30TtK9CFD0AEriID2iGjbdGhcfa0aLQ130_provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP11315.RAaPqgD_sQLsEF4Ejga-_jeU9F1AsxSWBM0S_vyeNjVII130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11315.RAaPqgD_sQLsEF4Ejga-_jeU9F1AsxSWBM0S_vyeNjVII130_provenance.
• NP11149.RAD9uz6aKDgPZJwZ7KXk9-awzb8rpfMirrNCVBN-jjWwE130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11149.RAD9uz6aKDgPZJwZ7KXk9-awzb8rpfMirrNCVBN-jjWwE130_provenance.
• NP1446.RAv7C_mZLpv3HZV9LJz6xuuA0v1t25ZWvm8C8yGR6cyyc130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1446.RAv7C_mZLpv3HZV9LJz6xuuA0v1t25ZWvm8C8yGR6cyyc130_provenance.
• NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_provenance.
• NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319838.RAho7d-25ISn0dKy-LmUo7irFgpiE60o-xJ3qOjevtgOE130_provenance.
• NP11316.RAEJDwequNDik7tVIFoRvZpvkFKNQIoo81RIMWRV0Y684130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11316.RAEJDwequNDik7tVIFoRvZpvkFKNQIoo81RIMWRV0Y684130_provenance.
• NP1447.RA54_2ROlIC8IYB35zYu-VGKv-Wyt4hNt3MLiZ4hw7yBU130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1447.RA54_2ROlIC8IYB35zYu-VGKv-Wyt4hNt3MLiZ4hw7yBU130_provenance.
• NP11314.RAx0OQ-YgDfzggFipEdooE05E7zqS6ZwDsG99FCyMcuIo130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11314.RAx0OQ-YgDfzggFipEdooE05E7zqS6ZwDsG99FCyMcuIo130_provenance.
• NP319839.RA35MxcD09mEaBNKZMqmda-uqnJvCBa8AdBH87qUSi37k130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319839.RA35MxcD09mEaBNKZMqmda-uqnJvCBa8AdBH87qUSi37k130_provenance.