Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP308496.RAiHIoY5P8RatRaQ1JmJeIb8yJ-0_p2kCIeZxkdCBJP30130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308496.RAiHIoY5P8RatRaQ1JmJeIb8yJ-0_p2kCIeZxkdCBJP30130_provenance.
• NP821890.RAkpgXnP_Tjm7OJVYBc-bTlWoCiOxUPUia3zkY6KqIdo4130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821890.RAkpgXnP_Tjm7OJVYBc-bTlWoCiOxUPUia3zkY6KqIdo4130_provenance.
• NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_provenance.
• NP349488.RAEsCVCX7ruJYwksZOvX5b_satginpIeRFm1O0Xh23Cog130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349488.RAEsCVCX7ruJYwksZOvX5b_satginpIeRFm1O0Xh23Cog130_provenance.
• NP649185.RAR6h7JrnEvRa3ufkaQ0VeLGPxems2dDslno-TTfin4cE130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649185.RAR6h7JrnEvRa3ufkaQ0VeLGPxems2dDslno-TTfin4cE130_provenance.
• NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_provenance.
• NP1347073.RACXOZ0Qc4Lu7T-IGIWfY9TpFQ1nIQk4RokxXuvYjqTCM130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1347073.RACXOZ0Qc4Lu7T-IGIWfY9TpFQ1nIQk4RokxXuvYjqTCM130_provenance.
• NP1347076.RAoWjzW8vS1LDsxa-pl5x7oyaBagZ5EFiy6ywhYLTlv-4130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1347076.RAoWjzW8vS1LDsxa-pl5x7oyaBagZ5EFiy6ywhYLTlv-4130_provenance.
• NP674080.RAMNqspsAn6PhvZOAvX6lQDbD6Hdeqv2ZTA3wFY4PWsI0130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674080.RAMNqspsAn6PhvZOAvX6lQDbD6Hdeqv2ZTA3wFY4PWsI0130_provenance.
• NP1347074.RAJTBtvlJfk08Hp-nu7kdgZEQExMVhHwzZBGaLaiE3m4U130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1347074.RAJTBtvlJfk08Hp-nu7kdgZEQExMVhHwzZBGaLaiE3m4U130_provenance.
• NP1347075.RAEPRqawTVEt7Npc8YKGL06z-uWE1p9dViXsPlWAzSRY0130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1347075.RAEPRqawTVEt7Npc8YKGL06z-uWE1p9dViXsPlWAzSRY0130_provenance.