Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP795894.RASgCUy3DvQpv2_l1fey6gMzwngKIYt0GK-TtEdKsfhQM130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795894.RASgCUy3DvQpv2_l1fey6gMzwngKIYt0GK-TtEdKsfhQM130_provenance.
• NP465411.RAeQyeL2UgVr6L2LgIkROmbH2tPctXYgsTsiQy_35DrAc130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465411.RAeQyeL2UgVr6L2LgIkROmbH2tPctXYgsTsiQy_35DrAc130_provenance.
• NP320172.RABJszjbFsrzsirRtpO2ztIlXuW0aBxvwfKK4OLL396ew130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320172.RABJszjbFsrzsirRtpO2ztIlXuW0aBxvwfKK4OLL396ew130_provenance.
• NP239795.RA_SR_A8rkuVYWXT3b5a7u8tUmhsTnVmA2Bfazj-o6FU0130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239795.RA_SR_A8rkuVYWXT3b5a7u8tUmhsTnVmA2Bfazj-o6FU0130_provenance.
• NP805078.RAKpN0nZn_f8qn6SgClouHkgJLjpPteo9DFfnKNgXdmnE130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805078.RAKpN0nZn_f8qn6SgClouHkgJLjpPteo9DFfnKNgXdmnE130_provenance.
• NP872650.RAEAT4_w1U4FOT2qNZJAMkU_JJEfwOG-4Mopgn7VvC4HI130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872650.RAEAT4_w1U4FOT2qNZJAMkU_JJEfwOG-4Mopgn7VvC4HI130_provenance.
• NP320075.RA-F4jSrDNO3jR56yYoZEll04yU8R-v74gHSDFT96BiEQ130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320075.RA-F4jSrDNO3jR56yYoZEll04yU8R-v74gHSDFT96BiEQ130_provenance.
• assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP526827.RA3aCaP-zpr_CSOYYoQYL6ay9nENlBo3W2HLzo4u4Bp6U130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526827.RA3aCaP-zpr_CSOYYoQYL6ay9nENlBo3W2HLzo4u4Bp6U130_provenance.
• NP526828.RAwFHjM6-ZrYAfSKtsufxa-Bih6om8u0eY2l6zdfKVFK8130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526828.RAwFHjM6-ZrYAfSKtsufxa-Bih6om8u0eY2l6zdfKVFK8130_provenance.
• NP526830.RAR_Fdn3yQpwnUa9fhTiFV685r-wQUfXWXJyDdYv-44K4130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526830.RAR_Fdn3yQpwnUa9fhTiFV685r-wQUfXWXJyDdYv-44K4130_provenance.
• NP526829.RAPaeexZzPoRMp-6hwgEGW48hWgV1WO3xp8jm4qR1gRsY130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526829.RAPaeexZzPoRMp-6hwgEGW48hWgV1WO3xp8jm4qR1gRsY130_provenance.
• NP320059.RAjCkt1YXN45HGycbljyOfd4Ir55MKt7AWnzO5aGu1n0E130_assertion description "[Mutations in the COL4A5 collagen gene have been implicated as the primary defect in Alport syndrome, a heritable disorder characterized by sensorineural deafness and glomerulonephritis that progresses to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320059.RAjCkt1YXN45HGycbljyOfd4Ir55MKt7AWnzO5aGu1n0E130_provenance.