Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_assertion description "[Our data showed that the F2 homozygous Gpdx mutant with C57L/J background exhibiting the G6PD activity was 0.9�0.1 U/g Hb, level similar to those of G6PD deficiency in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_assertion evidence source_evidence_literature NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_assertion SIO_000772 21839656 NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_assertion wasDerivedFrom befree-2016 NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_assertion wasGeneratedBy ECO_0000203 NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP916864.RAbj1FQTGa0O8Pil169D6n14-sZL5OnAlJ8IeXMxI0YJQ130_provenance.