Matches in Nanopublications for { ?s ?p "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP718800.RACrYNQISvtPB-lJe-N5AfH5PqbmpVUJJlWy8cTst0kVM130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718800.RACrYNQISvtPB-lJe-N5AfH5PqbmpVUJJlWy8cTst0kVM130_provenance.
- NP718797.RApf7IKTbO5bMtyCm75pbi9UloRr3dWfWJBSp5PxISE-A130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718797.RApf7IKTbO5bMtyCm75pbi9UloRr3dWfWJBSp5PxISE-A130_provenance.
- NP873970.RAwVNQeu828dKjbdKndBUnOcmnUliBPxetZ_-NsfvW55A130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873970.RAwVNQeu828dKjbdKndBUnOcmnUliBPxetZ_-NsfvW55A130_provenance.
- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_provenance.