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- NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_assertion type Assertion NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_head.
- 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.
- NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_assertion evidence source_evidence_literature NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_provenance.
- NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_assertion SIO_000772 22095278 NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_provenance.
- NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_assertion wasDerivedFrom befree-20140225 NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_provenance.
- NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_assertion wasGeneratedBy ECO_0000203 NP505180.RAVKeT_mGvVVZA5BHoKEFe6k34neAdnjusSxO06NHAdjg130_provenance.