Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_assertion description "[We describe mutations in the PML nuclear body protein Sp110 in the syndrome veno-occlusive disease with immunodeficiency, an autosomal recessive disorder of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_assertion evidence source_evidence_literature NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_assertion SIO_000772 16648851 NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_assertion wasDerivedFrom befree-20140225 NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_assertion wasGeneratedBy ECO_0000203 NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925280.RAkkqzmX2DBs5FLCGOtGiW17lHQcT5gCHuR0jiVxQQ3FA130_provenance.