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- source_evidence_literature type ECO_0000212 NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_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.
- NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_assertion evidence source_evidence_literature NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
- NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_assertion SIO_000772 22095278 NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
- NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_assertion wasDerivedFrom befree-20150227 NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
- NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_assertion wasGeneratedBy ECO_0000203 NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP844246.RAkHaRc8uCuUkwm0cCMVYkNs8uE8p0oquDIfiPxdJiX-M130_provenance.