Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_assertion description "[Mutations or deletions in the SH2D1A (src homology 2 domain protein 1A) gene result in a severe immunodeficiency called X-linked lymphoproliferative (XLP) disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_assertion evidence source_evidence_literature NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_assertion SIO_000772 12224001 NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_assertion wasDerivedFrom befree-20140225 NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_assertion wasGeneratedBy ECO_0000203 NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP186559.RAFbe8MZeKiUz5Dk4x0c4MFHk0fbAPPObRI49o0NGtA8E130_provenance.