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- source_evidence_literature type ECO_0000212 NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_assertion description "[Classical citrullinemia (CTLN1) is an inborn error of the urea cycle caused by reduced/abolished activity of argininosuccinate synthetase due to mutations in the ASS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_assertion evidence source_evidence_literature NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_assertion SIO_000772 25179242 NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_assertion wasDerivedFrom befree-2016 NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_assertion wasGeneratedBy ECO_0000203 NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216032.RA1IWwyWYKVdbfYrpfY-G_yD0jNz3pJ826PO8yPoAVXE0130_provenance.