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- source_evidence_literature type ECO_0000212 NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_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." NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_assertion evidence source_evidence_literature NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_assertion SIO_000772 14729329 NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_assertion wasDerivedFrom befree-20150227 NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_assertion wasGeneratedBy ECO_0000203 NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810573.RAmtGR0lOwej_xek4y7LFhWr7Ob0-SCIrPyBaOn5nEuWs130_provenance.