Matches in Nanopublications for { ?s ?p "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- NP578478.RAJP6sBsVAXBhf8_B3d8YdsamluLJeg-46vf0tM77pf-M130_assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578478.RAJP6sBsVAXBhf8_B3d8YdsamluLJeg-46vf0tM77pf-M130_provenance.
- assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_provenance.
- NP816240.RAEQ2BBOMStZ18INRAtYg4Fjy5l9GWqEtHDpgrIySSoS4130_assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816240.RAEQ2BBOMStZ18INRAtYg4Fjy5l9GWqEtHDpgrIySSoS4130_provenance.