Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_assertion description "[Molybdenum cofactor deficiency and isolated sulfite oxidase deficiency are autosomal recessive inborn errors of metabolism with severe neurological symptoms resulting from a lack of sulfite oxidase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_assertion evidence source_evidence_literature NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_assertion SIO_000772 12533804 NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_assertion wasDerivedFrom befree-20140225 NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_assertion wasGeneratedBy ECO_0000203 NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505149.RAHMb176h59VdvlQuY3DmL6kkZpsAJPOKbSxZ6qZ76mtM130_provenance.