Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP412524.RAr5L9P5MgP3jMOSHLHabI01lCDOJtR11kqsUZOdT5vAI130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412524.RAr5L9P5MgP3jMOSHLHabI01lCDOJtR11kqsUZOdT5vAI130_provenance.
• NP782804.RACRI1M06AjoEF3ATHPadq87p0snE5EZ4DSIgtrVsPUoU130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782804.RACRI1M06AjoEF3ATHPadq87p0snE5EZ4DSIgtrVsPUoU130_provenance.
• NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
• NP504365.RAQIR9vhcVsVkJEq1r3om5xHLQJZxk8GyIGlcdrSvt7Zs130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504365.RAQIR9vhcVsVkJEq1r3om5xHLQJZxk8GyIGlcdrSvt7Zs130_provenance.
• NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_provenance.
• NP418936.RA4-GVfXGFDqHdF9BsEbcvm54s81cGjoP2ZABtW9RLV0c130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418936.RA4-GVfXGFDqHdF9BsEbcvm54s81cGjoP2ZABtW9RLV0c130_provenance.
• NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
• NP460736.RAw0Em1FcIJCMTukNMTmgj_qEAWntFhgm1zlKpQFNNin8130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460736.RAw0Em1FcIJCMTukNMTmgj_qEAWntFhgm1zlKpQFNNin8130_provenance.
• assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP286505.RAjNn6nqgRVDAd8mZSA0qhw1nMQE73L7P_4_LGGLuxfsk130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286505.RAjNn6nqgRVDAd8mZSA0qhw1nMQE73L7P_4_LGGLuxfsk130_provenance.
• NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
• NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_provenance.
• NP915866.RAr4iYr5CPRVJei4i0ravHS_olnbBG5a9cGje4cV4A2JM130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915866.RAr4iYr5CPRVJei4i0ravHS_olnbBG5a9cGje4cV4A2JM130_provenance.