Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_assertion description "[Heterozygous mutations in CD95, CD95 ligand or caspase-10 underlie most cases of autoimmune lymphoproliferative syndrome (ALPS), a human disorder that is characterized by defective lymphocyte apoptosis, lymphadenopathy, splenomegaly and autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_assertion evidence source_evidence_literature NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_assertion SIO_000772 12353035 NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_assertion wasDerivedFrom befree-20140225 NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_assertion wasGeneratedBy ECO_0000203 NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478446.RAd75cwPq6X_sGl4UpGi31qW9aOrFNXajXjVkFcYJXzzw130_provenance.