Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_assertion description "[Among primary HLH-related genes, SH2D1A and XIAP are genetically responsible for X-linked lymphoproliferative syndrome (XLP) due to signaling-lymphocytic-activation-molecule-associated protein (SAP) and XIAP deficiencies, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_assertion evidence source_evidence_literature NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_assertion SIO_000772 22672194 NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_assertion wasDerivedFrom befree-2016 NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_assertion wasGeneratedBy ECO_0000203 NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.
- befree-2016 importedOn "2016-02-19" NP987543.RAuMEekgWqhrvA9yg7GRsl61mf9b1gG4i_KuoQ_e0hPlU130_provenance.