Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion description "[K(ATP) channel mutations were most common (15%) followed by GLUD1 mutations causing hyperinsulinism with hyperammonemia (5.9%), and HNF4A mutations (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion evidence source_evidence_literature NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion SIO_000772 20164212 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion wasDerivedFrom gad-20150221 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_assertion wasGeneratedBy ECO_0000203 NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP138084.RAGZnicm9zMLtK4RjBnwrrWcCRFLTIk-W716NCrX8MGZI130_provenance.