Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- befree-2016 importedOn "2016-02-19" NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_assertion wasGeneratedBy ECO_0000203 NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_assertion wasDerivedFrom befree-2016 NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_assertion SIO_000772 18425437 NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_assertion evidence source_evidence_literature NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.
- NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_assertion description "[Deficiency of dihydropteridine reductase causes a variant form of phenylketonuria associated with a devastating neurological disease characterized by mental retardation, hypokinesis and other features relating to basal ganglia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666975.RApDCT-EOkHvJxkHOLgFL-N6xUjkWF-IXJ4yoo5IK1g3U130_provenance.