Matches in Nanopublications for { ?s ?p "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_provenance.
- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_provenance.
- NP294152.RAgpRvXcssYijqB8GrR8n5XGm_SEOUBY9JXLs4cw_2FoY130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294152.RAgpRvXcssYijqB8GrR8n5XGm_SEOUBY9JXLs4cw_2FoY130_provenance.
- NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- NP294150.RA4nSMbLAZ0hpQzWdJWij43WwaiVIodc3O4BluV11l5uA130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294150.RA4nSMbLAZ0hpQzWdJWij43WwaiVIodc3O4BluV11l5uA130_provenance.