Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_assertion wasGeneratedBy ECO_0000203 NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_assertion wasDerivedFrom befree-20140225 NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_assertion SIO_000772 15802217 NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_assertion evidence source_evidence_literature NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_assertion description "[Alanine:glyoxylate aminotransferase-1 (AGT) is a human liver peroxisomal enzyme whose deficiency results in, primary hyperoxaluria type 1 (PH1), a fatal metabolic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP793568.RACkrZ47R53b_1sf9d_9Ide29Ux7UJ7mBIJwDsiZju8Dc130_provenance.