Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_assertion description "[GAP-43 levels were low in all disorders analysed (in particular motor neuron disease; p=0.001, and movement disorders and multiple sclerosis; p<0.0001) compared to controls, aside from CNS infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_assertion evidence source_evidence_literature NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_assertion SIO_000772 25175067 NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_assertion wasDerivedFrom befree-2016 NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_assertion wasGeneratedBy ECO_0000203 NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215596.RAEF7dibp-Y0KEti-QQwaip0VBjSyzGhD-G6zkXjPZ-a0130_provenance.