Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_assertion description "[The patients with subtypes CDG-Ia and CDG-Ib have mutations in the genes encoding phosphomannomutase 2 (PMM2) and phosphomannose isomerase (MPI or PMI), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_assertion evidence source_evidence_literature NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_assertion SIO_000772 21949237 NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_assertion wasDerivedFrom befree-20140225 NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_assertion wasGeneratedBy ECO_0000203 NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP621504.RA8wF9eZA_4Rtq2_fPSvucLHZnzYuqYl9DvZXOAreVOzI130_provenance.