Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_assertion description "[A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_assertion evidence source_evidence_literature NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_assertion SIO_000772 11201367 NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_assertion wasDerivedFrom befree-20150227 NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_assertion wasGeneratedBy ECO_0000203 NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433911.RAr9EV0ela_gPA0_Ho7kclIt7Wx2J0utTw6cFzwV38TRQ130_provenance.