Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP320197.RAAzVwlY_FmH_Z2FbYF92efaIFWfGVYyeay8z2zi0cdDM130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320197.RAAzVwlY_FmH_Z2FbYF92efaIFWfGVYyeay8z2zi0cdDM130_provenance.
• NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_provenance.
• NP320227.RASwx4fnmZkjD5UBAySxlaXfl2f0YVp_E3Pr65AMiiSmc130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320227.RASwx4fnmZkjD5UBAySxlaXfl2f0YVp_E3Pr65AMiiSmc130_provenance.
• NP320064.RA9Yr_6Xkbus-Dfr2ksrfOEPkXybJqCrhOscgfDJn6mi8130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320064.RA9Yr_6Xkbus-Dfr2ksrfOEPkXybJqCrhOscgfDJn6mi8130_provenance.
• NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
• NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_provenance.
• assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_provenance.
• NP1081294.RA-y3TcoLqbBEa-Pzr6-aPj7b-E3FIMlwP1EZVUdyRf6k130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081294.RA-y3TcoLqbBEa-Pzr6-aPj7b-E3FIMlwP1EZVUdyRf6k130_provenance.
• NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_provenance.
• NP1081295.RAV_b2RQlLC5kX8ZBBY4u-QHZKOgZdWBrJfz9r24cYGvY130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081295.RAV_b2RQlLC5kX8ZBBY4u-QHZKOgZdWBrJfz9r24cYGvY130_provenance.
• NP320074.RAhNDDQSK7CLqinOChsQYNhIIZsTIXDQMLKE4sO9i_EwY130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320074.RAhNDDQSK7CLqinOChsQYNhIIZsTIXDQMLKE4sO9i_EwY130_provenance.
• NP1081298.RAN83oOXKtay5LwHYbOSGBBlWPW85cr24umEpZ2467PRg130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081298.RAN83oOXKtay5LwHYbOSGBBlWPW85cr24umEpZ2467PRg130_provenance.
• NP1081296.RAj8exvo5gNH1fkdOIm8D43A-iAkfjOjlqTQaHiMz1teY130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081296.RAj8exvo5gNH1fkdOIm8D43A-iAkfjOjlqTQaHiMz1teY130_provenance.
• NP1081297.RAo9Dy9jXLgnFwI84QH043zxvyoba-662Q77cpsGztjWk130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081297.RAo9Dy9jXLgnFwI84QH043zxvyoba-662Q77cpsGztjWk130_provenance.