Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP425033.RAVhDQeNSJYo7X_4mbOSxWLMK4G2sP12khNExM8PsEk9I130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425033.RAVhDQeNSJYo7X_4mbOSxWLMK4G2sP12khNExM8PsEk9I130_provenance.
• NP385021.RA4jyzA8-Mx8PKUGCftNy6X0vv9snPCZC1UsN3-KSThKk130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385021.RA4jyzA8-Mx8PKUGCftNy6X0vv9snPCZC1UsN3-KSThKk130_provenance.
• NP620808.RAhafOoON5y3kzrT4NmeLHa7GOLRcfwZGoljwm4WAhek4130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620808.RAhafOoON5y3kzrT4NmeLHa7GOLRcfwZGoljwm4WAhek4130_provenance.
• NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_provenance.
• assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP767563.RABqXuxx5hfpomcZR-QAlLf3wiffm-5I16Zu8WhbPuKKU130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767563.RABqXuxx5hfpomcZR-QAlLf3wiffm-5I16Zu8WhbPuKKU130_provenance.
• NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_provenance.
• NP478003.RAkiZcPt5UJju9x5a6ujSFmNz06oJL52G0aMfYGzm6C_4130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478003.RAkiZcPt5UJju9x5a6ujSFmNz06oJL52G0aMfYGzm6C_4130_provenance.
• NP478006.RAujtRmvqSKNr8Oe2S1QiYeS6OggMR0j_TydelyFWEF4Q130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478006.RAujtRmvqSKNr8Oe2S1QiYeS6OggMR0j_TydelyFWEF4Q130_provenance.
• NP954512.RAoPnniITTPIBgbbtOQfoitYM6iTmR6YvNsAA7ZynNpso130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954512.RAoPnniITTPIBgbbtOQfoitYM6iTmR6YvNsAA7ZynNpso130_provenance.
• NP478005.RA4-8Vm-wcBEg0iEMkDfc7viq5d6D_9XX62ZzpmoJXdVE130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478005.RA4-8Vm-wcBEg0iEMkDfc7viq5d6D_9XX62ZzpmoJXdVE130_provenance.
• NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.