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- source_evidence_literature type ECO_0000212 NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_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.
- NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_assertion evidence source_evidence_literature NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
- NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_assertion SIO_000772 22095278 NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
- NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_assertion wasDerivedFrom befree-20150227 NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
- NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_assertion wasGeneratedBy ECO_0000203 NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP970700.RAc5S0eSjohAnGzkE6qY9piGRE8hzKOacfozmnd28sK5w130_provenance.