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- source_evidence_literature type ECO_0000212 NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_assertion description "[Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_assertion evidence source_evidence_literature NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_assertion SIO_000772 12594532 NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_assertion wasDerivedFrom befree-20150227 NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_assertion wasGeneratedBy ECO_0000203 NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977363.RAnpaorJF8GZnltQWN7Osy36pVA8Dag-S9_7Upug68jRQ130_provenance.