Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_assertion description "[X-linked lymphoproliferative disease (XLP), a genetic disorder characterized by immunodeficiency to Epstein-Barr virus (EBV) infection, has been linked to mutations in the SH2D1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_assertion evidence source_evidence_literature NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_assertion SIO_000772 11493483 NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_assertion wasDerivedFrom gad-20130706 NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_assertion wasGeneratedBy ECO_0000203 NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.