Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_assertion description "[It has been discovered recently that mutations in subunits of eukaryotic initiation factor 2B (eIF2B) underlie the neurodegenerative disease termed 'vanishing white matter'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_assertion evidence source_evidence_literature NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_assertion SIO_000772 14729329 NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_assertion wasDerivedFrom befree-2016 NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_assertion wasGeneratedBy ECO_0000203 NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.
- befree-2016 importedOn "2016-02-19" NP428371.RAByVNBUwMKCfXRgsmUqIt459wkBI_W-cP8QRZjsMed74130_provenance.