Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_assertion description "[A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_assertion evidence source_evidence_literature NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_assertion SIO_000772 25439727 NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_assertion wasDerivedFrom befree-2016 NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_assertion wasGeneratedBy ECO_0000203 NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1241615.RA_vxNPYth840AbojfLfX9y6Uvl1om4bPLmEiS3E7xEsA130_provenance.