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- source_evidence_literature type ECO_0000212 NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_assertion description "[FOXG1B (forkhead box G1B) is a very intriguing candidate gene since it is known to promote neuronal progenitor proliferation and to suppress premature neurogenesis and its disruption is reported in a patient with postnatal microcephaly, corpus callosum agenesis, seizures, and severe mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_assertion evidence source_evidence_literature NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_assertion SIO_000772 18627055 NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_assertion wasDerivedFrom befree-2016 NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_assertion wasGeneratedBy ECO_0000203 NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.
- befree-2016 importedOn "2016-02-19" NP682136.RAnz7G0IKmozXo1qyInKm7pzzpxoTtJTIJNaXmoFu6ii8130_provenance.