Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_assertion wasGeneratedBy ECO_0000203 NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_assertion wasDerivedFrom befree-20150227 NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_assertion SIO_000772 17141632 NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_assertion evidence source_evidence_literature NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_assertion description "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.