Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_provenance.
• NP902586.RAVhbvyd5izGOotmgk6wnsk6bs0xBBzBMvIFzzz77IDkA130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902586.RAVhbvyd5izGOotmgk6wnsk6bs0xBBzBMvIFzzz77IDkA130_provenance.
• NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_provenance.
• NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
• assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_provenance.
• assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
• NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
• NP939727.RAu9rQv_Fp1gJORIncXfXyJFFBU2hj9NjVhGx1ZNe7cnA130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939727.RAu9rQv_Fp1gJORIncXfXyJFFBU2hj9NjVhGx1ZNe7cnA130_provenance.