Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_assertion description "[Mutations in eukaryotic initiation factor 2B (eIF2B) cause one of the most common leukodystrophies, childhood ataxia with CNS hypomyelination/vanishing white matter disease or CACH/VWM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_assertion evidence source_evidence_literature NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_assertion SIO_000772 16378743 NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_assertion wasDerivedFrom befree-2016 NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_assertion wasGeneratedBy ECO_0000203 NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP528468.RA5rP9B_HTZc5LIlFbu5icb2-gFdpfv8Oy37hWZLQHtRQ130_provenance.