Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_assertion description "[Ornithine transcarbamylase (OTC) deficiency, the most common urea cycle disorder, is associated with severe hyperammonemia accompanied by a high risk of neurological damage and death in patients presenting with the neonatal-onset form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_assertion evidence source_evidence_literature NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_assertion SIO_000772 19384294 NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_assertion wasDerivedFrom befree-20140225 NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_assertion wasGeneratedBy ECO_0000203 NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447818.RA9sT0DkPZNHDOu_dxaIfZgGNHMO76CqxZ7Tp39ZC9DWE130_provenance.