Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion> ?p ?o ?g. }
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- NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion type Assertion NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_head.
- 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.
- NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion evidence source_evidence_literature NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_provenance.
- NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion SIO_000772 22095278 NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_provenance.
- NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion wasDerivedFrom befree-2016 NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_provenance.
- NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_assertion wasGeneratedBy ECO_0000203 NP939725.RAdzk2n3zBqG0LVyekcbCLb5OpLh9SX594KJn0-0gAbOk130_provenance.